Yan, Zhenguang et al. published their research in Science of the Total Environment in 2022 | CAS: 101-20-2

1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Electric Literature of C13H9Cl3N2O

Impairment of the gut health in Danio rerio exposed to triclocarban was written by Yan, Zhenguang;Du, Jinzhe;Zhang, Tianxu;Sun, Qianhang;Sun, Binbin;Zhang, Yan;Li, Shuo. And the article was included in Science of the Total Environment in 2022.Electric Literature of C13H9Cl3N2O This article mentions the following:

Triclocarban (TCC) is the principal component in personal and health care products because it is a highly effective, broad-spectrum, and safe antibacterial agent. TCC has recently been discovered in aquatic creatures and has been shown to constitute a health danger to aquatic animals. Although several studies have looked into the toxicol. effects of TCC on a variety of aquatic animals from algae to fish, the possible gut-toxicity mol. pathway in zebrafish has never been thoroughly explored. We investigated the gut-toxic effects of TCC on zebrafish by exposing them to different TCC concentrations (100 and 1000μg/L) for 21 days. We discovered for the first time that the MAPK and TLR signaling pathways related to gut diseases were significantly altered, and inflammation (up-regulation of TNF-α, IL-6, and IL-1β) caused by TCC was confirmed to be largely mediated by the aryl hydrocarbon receptor (AHR) and its related cytokines. This was found using the results of qPCR, a transcriptome anal., and mol. docking (AHR, AHRR, CYP1A1 and CYP1B1). Furthermore, high-throughput 16S rDNA sequencing demonstrated that TCC exposure reduced the bacterial diversity and changed the gut microbial composition, with the primary phyla Fusobacteria and Proteobacteria, as well as the genera Cetobacterium and Rhodobacteraceae, being the most affected. TCC exposure also caused damage to the gut tissue, including an increase in the number of goblet cells and a reduction in the height of the columnar epithelium and the thickness of the muscular layer, as shown by hematoxylin and eosin staining. Our findings will aid in understanding of the mechanism TCC-induced aquatic toxicity in aquatic species. In the experiment, the researchers used many compounds, for example, 1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2Electric Literature of C13H9Cl3N2O).

1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Electric Literature of C13H9Cl3N2O

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Fei, Zhaohui et al. published their research in Journal of Environmental Chemical Engineering in 2022 | CAS: 4422-95-1

Trimesoylchloride (cas: 4422-95-1) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Synthetic Route of C9H3Cl3O3

Imidazole assisted molecular-scale regulation of polyamide for preparing reverse osmosis membrane with enhanced water permeance was written by Fei, Zhaohui;Jiang, Chi;Li, Mengxin;Hou, Yingfei. And the article was included in Journal of Environmental Chemical Engineering in 2022.Synthetic Route of C9H3Cl3O3 This article mentions the following:

The development of reverse osmosis (RO) technol. is still hindered by many obstacles, especially the low water permeance of RO membrane. Herein, an interfacial polymerization regulated by N-acyl imidazole chem. was proposed to fabricate high permeance RO membranes. The improvement of membrane performance was achieved by simply adding 2-methylimidazole (Hmim) into aqueous phase. More angstrom-scale free volume elements, which acted as water mol. transport channels, were formed in the polyamide separation layer due to the reaction and hydrolysis of Hmim. As a result, a substantial increase in water permeance was achieved while maintaining high NaCl rejection. In addition, more carboxylic acid groups were formed on the membrane surface due to the hydrolysis of N-acyl imidazole, thereby imparting higher hydrophilicity and anti-fouling properties to the membrane. With the addition of 1.5 weight/weight% Hmim, the water permeance of the prepared RO membrane was improved to 4.4 L m-2 h-1 bar-1, nearly 4.5 times compared to the control group, while maintaining a high NaCl rejection of above 98%, thus successfully overcoming the permeability-selectivity trade-off limit. This work paves a new idea for the development of additives in the preparation of RO membranes. In the experiment, the researchers used many compounds, for example, Trimesoylchloride (cas: 4422-95-1Synthetic Route of C9H3Cl3O3).

Trimesoylchloride (cas: 4422-95-1) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Synthetic Route of C9H3Cl3O3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Pan, Zhentao et al. published their research in Green Chemistry in 2021 | CAS: 6590-96-1

2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Quality Control of 2,4-Dichlorophenylisothiocyanate

Eco-friendly construction of spiroquinazolin-2-(thi)ones and quinolin-(thio)ureas via Fe(III)-catalyzed multi-component domino double [4 + 2] annulations was written by Pan, Zhentao;Shi, Shuaijun;Yang, Xuancheng;Xiao, Xuqiong;Zhang, Wangqin;Wang, Shiliang;Ma, Yongmin. And the article was included in Green Chemistry in 2021.Quality Control of 2,4-Dichlorophenylisothiocyanate This article mentions the following:

An unprecedented eco-friendly multi-component domino approach for the synthesis of novel spiroquinazolin-2-(thi)ones I (X = O, S; R = H, Me; R1 = Me, Et; R2 = n-Pr, 4-fluorophenyl, 4-(ethoxycarbonyl)benzen-1-yl, etc.) and quinolin-(thio)ureas II (R3 = i-Pr, 2,4-dichlorophenyl, naphthalen-1-yl, etc.) is described. The protocol proceeds via domino double [4+2] annulations and features an eco-benign catalyst and solvent, simple starting materials, high atom-economy, H2O as the sole byproduct and a simple work-up procedure. In the experiment, the researchers used many compounds, for example, 2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1Quality Control of 2,4-Dichlorophenylisothiocyanate).

2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Quality Control of 2,4-Dichlorophenylisothiocyanate

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Hansa, Raj KC. et al. published their research in European Journal of Medicinal Chemistry in 2021 | CAS: 2613-34-5

3-Chloro-2,4-difluoroaniline (cas: 2613-34-5) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Computed Properties of C6H4ClF2N

4-4-(Anilinomethyl)-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-1-ylbenzoic acid derivatives as potent anti-gram-positive bacterial agents was written by Hansa, Raj KC.;Khan, M. M. K.;Frangie, M. M.;Gilmore, D. F.;Shelton, R. S.;Savenka, A. V.;Basnakian, A. G.;Shuttleworth, S. L.;Smeltzer, M. S.;Alam, M. A.. And the article was included in European Journal of Medicinal Chemistry in 2021.Computed Properties of C6H4ClF2N This article mentions the following:

A collection of potent antimicrobials consisting of novel 1,3-bis-benzoic acid and trifluoromethyl Ph derived pyrazoles I [R = HO(O)C, F3C; R1 = Ph, 3-bromophenyl, 5-iodopyridin-2-yl, etc.] was synthesized and tested for antibacterial activity. The majority of trifluoromethyl Ph derivatives are highly potent growth inhibitors of Gram-pos. bacteria and showed low toxicity to human cultured cells. In particular, two compounds I [R = F3C; R1 = 3-fluoro-5-(trifluoromethyl)phenyl, 3,5-dichloro-4-fluorophenyl] were selected for addnl. studies. These compounds were highly effective against Staphylococcus aureus as shown by a low min. inhibitory concentration (MIC), a bactericidal effect in time-kill assays, moderate inhibition of biofilm formation as well as biofilm destruction and a bactericidal effect against stationary phase cells representing non-growing persister cells. Multistep resistance assays showed a very low tendency for S. aureus and Enterococcus faecalis to develop resistance through mutation. Addnl., in vivo mouse model studies showed no harmful effects at doses up to 50 mg/kg using 14 blood plasma organ toxicity markers or TUNEL assay in liver and kidney. Investigations into the mode of action by performing macromol. synthesis inhibition studies showed a broad range of inhibitory effects, suggesting targets that have a global effect on bacterial cell function. In the experiment, the researchers used many compounds, for example, 3-Chloro-2,4-difluoroaniline (cas: 2613-34-5Computed Properties of C6H4ClF2N).

3-Chloro-2,4-difluoroaniline (cas: 2613-34-5) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Computed Properties of C6H4ClF2N

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Yu, Yi et al. published their research in Journal of Organic Chemistry in 2022 | CAS: 620-19-9

1-(Chloromethyl)-3-methylbenzene (cas: 620-19-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Synthetic Route of C8H9Cl

Electrochemical Sulfoxidation of Thiols and Alkyl Halides was written by Yu, Yi;Wu, Shao-Fen;Zhu, Xiao-Bin;Yuan, Yaofeng;Li, Zhen;Ye, Ke-Yin. And the article was included in Journal of Organic Chemistry in 2022.Synthetic Route of C8H9Cl This article mentions the following:

A green and efficient electrochem. sulfoxidation via the use of readily available materials, i.e., thiols and alkyl halides was reported. The simple operation, mild conditions and broad substrate scope render this protocol potentially applicable for the preparation of diverse synthetically significant sulfoxides RSOCH2R1 [R = i-Pr, 4-FC6H4, 4-ClC6H4, etc.; R1 = (CH2)2CH3, Ph, 3-MeOC6H4, etc.]. In the experiment, the researchers used many compounds, for example, 1-(Chloromethyl)-3-methylbenzene (cas: 620-19-9Synthetic Route of C8H9Cl).

1-(Chloromethyl)-3-methylbenzene (cas: 620-19-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Synthetic Route of C8H9Cl

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Rozaini, Muhammad Nur’ Hafiz et al. published their research in Microchemical Journal in 2021 | CAS: 101-20-2

1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Formula: C13H9Cl3N2O

Green adsorption-desorption of mixed triclosan, triclocarban, 2-phenylphenol, bisphenol A and 4-tert-octylphenol using MXene encapsulated polypropylene membrane protected micro-solid-phase extraction device in amplifying the HPLC analysis was written by Rozaini, Muhammad Nur’ Hafiz;Kiatkittipong, Worapon;Saad, Bahruddin;Yahaya, Noorfatimah;Shaharun, Maizatul Shima;Sangu, Sangeetha Siva;Mohamed Saheed, Mohamed Shuaib;Wong, Yong Foo;Mohamad, Mardawani;Sambudi, Nonni Soraya;Lim, Jun Wei. And the article was included in Microchemical Journal in 2021.Formula: C13H9Cl3N2O This article mentions the following:

The endocrine disruptor compounds (EDC) are inevitable hazardous pollutants usually found in the discharged wastewater effluents, polluting the natural water bodies. This can be rationalised by the ineffective anal. methods that fail to quantify EDC in the treated wastewaters, forestalling the advancement of wastewater treatment processes that could completely mineralize the EDC. Therefore, a novel polypropylene membrane protected micro-solid-phase extraction (μ-SPE) device was developed using MXene encapsulated sorbent in enhancing the anal. of mixed EDC, namely, triclosan, triclocarban, 2-phenylphenol, bisphenol A and 4-tert-octylphenol, via a high-performance liquid chromatog.-diode array detector approach. The green adsorption-desorption of EDC from polypropylene membrane protected μ-SPE device was optimized at sorbent loading of 2 mg, extraction time of 30 min, sodium chloride of 15% (w/v), medium pH of 8, a sample volume of 10 mL, desorption solvent of isopropanol, desorption time of 3 min and desorption solvent volume of merely 150μL. Under the optimum condition, the proposed method showed a good EDC detection limit ranging from 0.37 to 0.58μg L-1 with acceptable relative recoveries between 81.0% and 105.5%. Moreover, the calculated enrichment factors also confirmed the EDC selectivity by polypropylene membrane protected μ-SPE device followed triclosan > 4-tert-octylphenol > bisphenol A > triclocarban > 2-phenylphenol. Finally, the polypropylene membrane protected μ-SPE device was assessed using real water, and wastewater samples and the EDC of triclosan and 4-tert-octylphenol were detected in the municipal wastewater and lake water, resp. In the experiment, the researchers used many compounds, for example, 1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2Formula: C13H9Cl3N2O).

1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Formula: C13H9Cl3N2O

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Hu, Jiahui et al. published their research in Separation and Purification Technology in 2022 | CAS: 4422-95-1

Trimesoylchloride (cas: 4422-95-1) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Related Products of 4422-95-1

Solvent-resistant polyimide aerogel film as ultrapermeable support for thin-film composite and covalent organic framework nanofiltration membranes was written by Hu, Jiahui;Kumar, Sushil;Hardian, Rifan;Yang, Cong;Szekely, Gyorgy. And the article was included in Separation and Purification Technology in 2022.Related Products of 4422-95-1 This article mentions the following:

Organic solvent nanofiltration (OSN) membranes require robust selective layers and support materials. In this study, polyamide and polyester thin-film composites (TFCs) and covalent organic frameworks (COFs) were fabricated as selective layers on a polyimide aerogel support. The ultrapermeable support was stable in various organic solvents including harsh polar aprotic solvents such as N,N-dimethylformamide (DMF), dimethylsulfoxide, N,N-dimethylacetamide, and N-methyl-2-pyrrolidone for more than six months. The support enabled fabricating both amorphous and crystalline selective layers at both room and higher temperatures Moreover, the polyimide aerogel support had 85% porosity, facilitating high solvent flux. The compatibility of the selective layers and support was excellent, and as low mol. weight cutoff values (MWCO) as 356 and as high as 591 g mol-1 were obtained in methanol at 10 bar for the COFs and polyester TFC membranes, resp. Both exptl. MWCO and permeance values of the COF membrane agreed with those predicted using the pore flow model. The effect of the operating temperature on the OSN performance was examined in DMF at 20 and 100 °C. Both membranes demonstrated constant permeance and rejection for more than nine days of continuous filtration. In the experiment, the researchers used many compounds, for example, Trimesoylchloride (cas: 4422-95-1Related Products of 4422-95-1).

Trimesoylchloride (cas: 4422-95-1) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Related Products of 4422-95-1

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Kroth, Heiko et al. published their research in Bioorganic & Medicinal Chemistry in 2021 | CAS: 76-83-5

(Chloromethanetriyl)tribenzene (cas: 76-83-5) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Reference of 76-83-5

Structure-activity relationship around PI-2620 highlights the importance of the nitrogen atom position in the tricyclic core was written by Kroth, Heiko;Oden, Felix;Serra, Andreia Monica;Molette, Jerome;Mueller, Andre;Berndt, Mathias;Capotosti, Francesca;Gabellieri, Emanuele;Schmitt-Willich, Heribert;Hickman, David;Pfeifer, Andrea;Dinkelborg, Ludger;Stephens, Andrew. And the article was included in Bioorganic & Medicinal Chemistry in 2021.Reference of 76-83-5 This article mentions the following:

Tau aggregates represent a critical pathol. in Alzheimers disease (AD) and other forms of dementia. The extent of Tau neurofibrillary tangles across defined brain regions corresponds well to the observed level of cognitive decline in AD. Compound 1 (PI-2620) was recently identified as a promising Tau positron emission tomog. tracer for AD and non-AD tauopathies. To evaluate the impact of the N-atom position with respect to Tau- and off-target binding, tricyclic core analogs of PI-2620 with nitrogen atoms at different positions were prepared Affinity to aggregated Tau was evaluated using human AD brain homogenates, and their off-target binding was evaluated in a monoamine oxidase A (MAO-A) competition assay. The novel tricyclic core derivatives all displayed inferior Tau binding or MAO-A off-target selectivity, indicating PI-2620 to be the optimal design for high affinity binding to Tau and high MAO-A selectivity. In the experiment, the researchers used many compounds, for example, (Chloromethanetriyl)tribenzene (cas: 76-83-5Reference of 76-83-5).

(Chloromethanetriyl)tribenzene (cas: 76-83-5) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Reference of 76-83-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Bevan, Cecil W. L. et al. published their research in Nigerian Journal of Science in 1966 | CAS: 4815-64-9

1-Chloro-3-fluoro-5-nitrobenzene (cas: 4815-64-9) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Synthetic Route of C6H3ClFNO2

Aromatic nucleophilic substitution. XI. Effect of meta substituents was written by Bevan, Cecil W. L.;Hirst, J.;Una, S. J.. And the article was included in Nigerian Journal of Science in 1966.Synthetic Route of C6H3ClFNO2 This article mentions the following:

Variation in the rates and log B factor in the Arrhenius equation K = BE-/RT are recorded and correlated largely with changes in activation energy. The compounds used are 3-(R-substituted)-5-nitrofluorobenzenes with methoxide ion in methanol, R being NH2, CO2-, Me3, tert-Bu, OMe3, H, Ac, F, I, Cl, Br, CF3, SO2Me, or NO2. OMe and NH2 groups induce deactivation whereas Ac induces (-T) effect in the mol. MeSO2 in the para position is 10 times less activating than the NO2 group in the identical position. The trifluoromethyl group is found to induce an inductive effect while the CO2- group is weakly deactivating from the ortho position. As expected the effect of halogens in the meta position is powerfully accelerating. 34 references. In the experiment, the researchers used many compounds, for example, 1-Chloro-3-fluoro-5-nitrobenzene (cas: 4815-64-9Synthetic Route of C6H3ClFNO2).

1-Chloro-3-fluoro-5-nitrobenzene (cas: 4815-64-9) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Synthetic Route of C6H3ClFNO2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Funcke, A. B. H. et al. published their research in Arzneimittel-Forschung in 1956 | CAS: 7476-66-6

Methyl 2-chloro-2-phenylacetate (cas: 7476-66-6) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Application In Synthesis of Methyl 2-chloro-2-phenylacetate

Studies on spasmolytics. III. Influence of structural changes in nitrogen-free esters with spasmolytic activity was written by Funcke, A. B. H.;Rekker, R. F.;Ernsting, M. J. E.;Nauta, W. Th.. And the article was included in Arzneimittel-Forschung in 1956.Application In Synthesis of Methyl 2-chloro-2-phenylacetate This article mentions the following:

The following esters of α-chlorophenylacetic acid were prepared from the acyl chloride and resp. alc. (b.°/mm., nD20 and yield in % are given): Me 123-6/11, 1.4963, 60; Et 132-3/15, 1.5037, 65; Pr 140-2/19, 1.5024, 55; iso-Pr 125-30/8, 1.5010, 55; Bu 143-5/8, 1.4960, 65; iso-Bu 135-40/8, 1.4958, 30; Am 143-5/11 1.5028, 79; 2-Me-1-Bu 144-6/11, 1.5028, 81; 3-Me-1-Bu 145-7/11, 1.5029, 55; 2,2-dimethylpropyl 141-3/11, 1.4983, 68; 2-pentyl 144-5/11, 1.5023, 78; 2-Me-2-Bu 148-50/12, m. 70-2°, 83; 3-Me-2-Bu 146-8/12, 1.5018, 90; 3-pentyl 144-5/11, 1.5035, 69; 3,3,5-trimethyl-1-cyclohexyl 140/0.04, 1.5135, 81. The lower esters of the series have a higher spasmolytic activity than the corresponding mandelates; as the number of C atoms in the ester group increases, however, this relation is inversed. The following esters of phenylglyoxylic acid have little or no spasmolytic activity: 2-Me-1-Bu 118/0.02, 1.5058, 53; 1-heptyl 128/0.03, 1.4980, 61; 2,6-dimethyl-4-heptyl 125/0.05, 1.4900, 55; 3,3,5-trimethyl-1-cyclohexyl 145/0.05, m. 43-4°, 77. In the experiment, the researchers used many compounds, for example, Methyl 2-chloro-2-phenylacetate (cas: 7476-66-6Application In Synthesis of Methyl 2-chloro-2-phenylacetate).

Methyl 2-chloro-2-phenylacetate (cas: 7476-66-6) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Application In Synthesis of Methyl 2-chloro-2-phenylacetate

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics