Chen, Jinyi’s team published research in Journal of Chemical Thermodynamics in 2021 | CAS: 350-30-1

3-Chloro-4-fluoronitrobenzene(cas: 350-30-1) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties. Organochlorine compounds have wide use in many applications, though some are of profound environmental concern, with TCDD being one of the most notorious.Related Products of 350-30-1

Related Products of 350-30-1On March 31, 2021, Chen, Jinyi; Wang, Hongxing published an article in Journal of Chemical Thermodynamics. The article was 《Density, viscosity, and saturated vapour pressure of 3-chloro-4-fluoronitrobenzene and 3-chloro-2-fluoronitrobenzene》. The article mentions the following:

D. and viscosity data of pure 3-chloro-4-fluoronitrobenzene and 3-chloro-2-fluoronitrobenzene were obtained in temperature range from 318.15 K to 348.15 K at the local atm. pressure of 99.7 kPa. The value of corresponding saturated vapor pressure of two isomers were determined in the temperature range of 409 K to 517 K. The relationship between temperature and d. can be well correlated by the linear equation. The viscosity data was well described by the Litovitz, Ghatee, VFT, and Andrade equations, and the calculated value by the VFT equation is consistent with the measured data. Both the Antoine and Riedel equations can accurately describe the relationship between saturated vapor pressure and temperature of 3-chloro-4-fluoronitrobenzene and 3-chloro-2-fluoronitrobenzene, which can meet the requirements for chem. design. In addition, the thermal expansion coefficient was determined based on the d. data, and the molar vaporisation enthalpy of two isomers was evaluated using the Clausius-Clapeyron equation. In the experimental materials used by the author, we found 3-Chloro-4-fluoronitrobenzene(cas: 350-30-1Related Products of 350-30-1)

3-Chloro-4-fluoronitrobenzene(cas: 350-30-1) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties. Organochlorine compounds have wide use in many applications, though some are of profound environmental concern, with TCDD being one of the most notorious.Related Products of 350-30-1

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

Wacker, Dean A.’s team published research in Journal of Medicinal Chemistry in 2007 | CAS: 654-98-8

5-Chloro-2-(trifluoromethyl)benzoic acid(cas: 654-98-8) belongs to organochlorine compounds. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Safety of 5-Chloro-2-(trifluoromethyl)benzoic acid

Safety of 5-Chloro-2-(trifluoromethyl)benzoic acidOn March 22, 2007, Wacker, Dean A.; Varnes, Jeffrey G.; Malmstrom, Sarah E.; Cao, Xueying; Hung, Chen-Pin; Ung, Thao; Wu, Ginger; Zhang, Ge; Zuvich, Eva; Thomas, Michael A.; Keim, William J.; Cullen, Mary Jane; Rohrbach, Kenneth W.; Qu, Qinling; Narayanan, Rangaraj; Rossi, Karen; Janovitz, Evan; Lehman-McKeeman, Lois; Malley, Mary F.; Devenny, James; Pelleymounter, Mary Ann; Miller, Keith J.; Robl, Jeffrey A. published an article in Journal of Medicinal Chemistry. The article was 《Discovery of (R)-9-Ethyl-1,3,4,10b-tetrahydro-7-trifluoromethylpyrazino[2,1-a]isoindol- 6(2H)-one, a Selective, Orally Active Agonist of the 5-HT2C Receptor》. The article mentions the following:

Robust pharmaceutical treatment of obesity has been limited by the undesirable side-effect profile of currently marketed therapies. The synthesis and optimization of a class of pyrazinoisoindolone-containing, selective 5-HT2C agonists as antiobesity agents, are described. Key to optimization of the pyrazinoisoindolone core was the identification of the appropriate substitution pattern and functional groups which led to the discovery of compound I, a 5-HT2C agonist with >300-fold functional selectivity over 5-HT2B and >70-fold functional selectivity over 5-HT2A. Oral dosing of I reduced food intake in an acute rat feeding model, which could be completely reversed by a selective 5-HT2C antagonist and caused a reduction in body weight gain in a 4-day rat model. In the experimental materials used by the author, we found 5-Chloro-2-(trifluoromethyl)benzoic acid(cas: 654-98-8Safety of 5-Chloro-2-(trifluoromethyl)benzoic acid)

5-Chloro-2-(trifluoromethyl)benzoic acid(cas: 654-98-8) belongs to organochlorine compounds. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Safety of 5-Chloro-2-(trifluoromethyl)benzoic acid

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

Emami, Leila’s team published research in Journal of Heterocyclic Chemistry in 2022 | CAS: 620-20-2

3-Chlorobenzylchloride(cas: 620-20-2) has been used in the reaction of 3-methoxybenzyl chloride and ethyl 4-bromobenzoate in pure water, using zinc dust and a Pd catalyst.Synthetic Route of C7H6Cl2

Emami, Leila; Khabnadideh, Soghra; Faghih, Zahra; Solhjoo, Aida; Malek, Saba; Mohammadian, Amir; Divar, Masoumeh; Faghih, Zeinab published an article in Journal of Heterocyclic Chemistry. The title of the article was 《Novel N-substituted isatin-ampyrone Schiff bases as a new class of antiproliferative agents: Design, synthesis, molecular modeling and in vitro cytotoxic activity》.Synthetic Route of C7H6Cl2 The author mentioned the following in the article:

Thirteen novel isatin-ampyrone Schiff bases derivatives such as I [X = H, Cl; R = H, 3-F, 4-OMe, etc.] were synthesized by the reaction of isatins and benzyl halides followed by condensation with ampyrone. In vitro cytotoxic activity of these new Schiff bases against three human tumor cell lines (MCF-7, A549, and SCOV3) as well as normal breast cell line (MCF-10A) were evaluated by MTT assay. Structure-activity relationship of the tested compounds revealed that chlorine group at C-5 position of the isatin ring significantly increased the cytotoxic activity. This study generally led to introduce a highly active mol. I [X = Cl; R = 3-Cl] with IC50 values of 5.12, 25.5, and 12.9μM, on MCF-7, A549, and SCOV3, resp. Furthermore, mol. docking studies of the synthesized compounds were also done to investigate their binding modes to toward VEGFR-2 and JNK3-MAP kinase as the main targets for isatin-containing anticancer agents. Binding free energy values of the compounds showed pos. correlation with their cytotoxic activities. To confirm the docking results, mol. docking simulations of potent compound I [X = Cl; R = 3-Cl] against VEGFR-2 and JNK3 MAP kinase were also performed. According to the cytotoxic results and in silico ADMET predictions together, I [X = Cl; R = 3-Cl] could be considered as a potent candidate for the future anticancer studies. In the experimental materials used by the author, we found 3-Chlorobenzylchloride(cas: 620-20-2Synthetic Route of C7H6Cl2)

3-Chlorobenzylchloride(cas: 620-20-2) has been used in the reaction of 3-methoxybenzyl chloride and ethyl 4-bromobenzoate in pure water, using zinc dust and a Pd catalyst.Synthetic Route of C7H6Cl2

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

Magid, L. J.’s team published research in Journal of Physical Chemistry B in 2000 | CAS: 10007-84-8

Sodium 2,6-dichlorobenzoate(cas: 10007-84-8) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties.Formula: C7H3Cl2NaO2 Organochlorine compounds have wide use in many applications, though some are of profound environmental concern, with TCDD being one of the most notorious.

Magid, L. J.; Han, Z.; Li, Z.; Butler, P. D. published an article in Journal of Physical Chemistry B. The title of the article was 《Tuning the Contour Lengths and Persistence Lengths of Cationic Micelles: The Role of Electrostatics and Specific Ion Binding》.Formula: C7H3Cl2NaO2 The author mentioned the following in the article:

Small-angle scattering was used to obtain detailed information on micellar contour lengths and persistence lengths, a measure of micellar flexibility, for mixed micelles of cetyltrimethylammonium 2,6-dichlorobenzoate and cetyltrimethylammonium chloride in H2O as a function of surfactant and salt concentrations and the relative amounts of the 2 counterions (the counterion inventory) at the micellar surface. Increasing amounts at the surface of the penetrating counterion of the pair, 2,6-dichlorobenzoate, lowers the 1-dimensional bending modulus of the micelles, making them more flexible. Micellar contour lengths exhibit a maximum with increasing amounts of 2,6-dichlorobenzoate at the micellar surface. This is understood in terms of decreases in the micellar end-cap energies, Ec, at high concentrations of penetrating counterion. By decreasing the effective micellar surface charge d., penetrating counterions also cause decreased contributions from electrostatic repulsion, Ee, which retard micellar growth. At low ionic strengths, this results in more extensive micellar growth upon addition of Na 2,6-dichlorobenzoate rather than NaCl. In the experiment, the researchers used Sodium 2,6-dichlorobenzoate(cas: 10007-84-8Formula: C7H3Cl2NaO2)

Sodium 2,6-dichlorobenzoate(cas: 10007-84-8) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties.Formula: C7H3Cl2NaO2 Organochlorine compounds have wide use in many applications, though some are of profound environmental concern, with TCDD being one of the most notorious.

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

Rios-Mera, Juan D.’s team published research in Food Research International in 2019 | CAS: 7647-14-5

Sodium chloride(cas: 7647-14-5) has been used for the preparation of tris buffered saline, phosphate buffered saline, MPM-2 (mitotic protein monoclonal 2) cell lysis buffer, immunoprecipitation wash buffer, LB (Luria-Bertani) media and dialysis buffer.Application In Synthesis of Sodium chloride

In 2019,Food Research International included an article by Rios-Mera, Juan D.; Saldana, Erick; Cruzado-Bravo, Melina L. M.; Patinho, Iliani; Selani, Miriam M.; Valentin, Dominique; Contreras-Castillo, Carmen J.. Application In Synthesis of Sodium chloride. The article was titled 《Reducing the sodium content without modifying the quality of beef burgers by adding micronized salt》. The information in the text is summarized as follows:

This study determined the effect of the incorporation of micronized salt on physicochem., yield and consumer’s sensory characteristics of beef burger. The micronized salt was obtained by sieving the com. salt in a 60-mesh stainless steel sieve. The com. (regular salt) and micronized salt presented differences in the mean size, size distribution and bulk d. Half of the amount of the micronized salt was mixed with pork back fat, and the other half was added to the meat batter in the beef burger manufacture A Pivot profile method was used with consumers to describe the sensory properties of the burger samples (ranging from 0.5% to 1.5% NaCl). The Pivot profile data revealed that treatments with 0.75% and 0.5% micronized salt were mainly characterized as dry, besides showing the highest cooking loss and diameter reduction However, beef burgers with 1.0% micronized salt and 1.5% regular salt had similar perceived salty taste. In terms of salt reduction, the results indicated that it would be possible to reduce salt from 1.5% to 1.0% when using micronized salt, without affecting the pH, color parameters, yield properties and some sensory characteristics of the burger, such as salty, tasty, juicy, fatty, and spicy. Therefore, this strategy promises great potential for industrial application in products that contain lipids in their composition, such as meat products. The results came from multiple reactions, including the reaction of Sodium chloride(cas: 7647-14-5Application In Synthesis of Sodium chloride)

Sodium chloride(cas: 7647-14-5) has been used for the preparation of tris buffered saline, phosphate buffered saline, MPM-2 (mitotic protein monoclonal 2) cell lysis buffer, immunoprecipitation wash buffer, LB (Luria-Bertani) media and dialysis buffer.Application In Synthesis of Sodium chloride

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

Paula, Marielle Maria de Oliveira’s team published research in Meat Science in 2019 | CAS: 7647-14-5

Sodium chloride(cas: 7647-14-5) has been used for the preparation of tris buffered saline, phosphate buffered saline, MPM-2 (mitotic protein monoclonal 2) cell lysis buffer, immunoprecipitation wash buffer, LB (Luria-Bertani) media and dialysis buffer.Related Products of 7647-14-5

In 2019,Meat Science included an article by Paula, Marielle Maria de Oliveira; Haddad, Gabriela de Barros Silva; Rodrigues, Lorena Mendes; Benevenuto, Augusto Aloisio Junior; Ramos, Alcineia de Lemos Souza; Ramos, Eduardo Mendes. Related Products of 7647-14-5. The article was titled 《Effects of PSE meat and salt concentration on the technological and sensory characteristics of restructured cooked hams》. The information in the text is summarized as follows:

The effects of the use of normal and pale, soft, and exudative (PSE) meat on the technol. and sensorial quality of restructured cooked hams elaborated with different salt contents (0.8, 1.2, 1.6, 2.0, and 2.4%) were investigated. A low salt content implied (P < .05) high cooking loss (6.27 vs 3.25%), expressive moisture and C* values and low hardness. Products elaborated with PSE meat had (P < .05) lower cohesiveness, energy to fracture and hue tone color and higher springiness than did samples elaborated with normal meat. Salty taste perception was slightly higher for the PSE meat-based products, which were also preferred by the assessors when salt contents lower than 1.6% were used. It was concluded that when PSE meat was used, the addition of 1.2% salt was sufficient to maintain the technol. and sensory characteristics of the restructured cooked hams.Sodium chloride(cas: 7647-14-5Related Products of 7647-14-5) was used in this study.

Sodium chloride(cas: 7647-14-5) has been used for the preparation of tris buffered saline, phosphate buffered saline, MPM-2 (mitotic protein monoclonal 2) cell lysis buffer, immunoprecipitation wash buffer, LB (Luria-Bertani) media and dialysis buffer.Related Products of 7647-14-5

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

Asthana, Sharad Kumar’s team published research in New Journal of Chemistry in 2020 | CAS: 5781-53-3

Methyl 2-chloro-2-oxoacetate(cas: 5781-53-3) belongs to acyl chlorides. Lacking the ability to form hydrogen bonds, acyl chlorides have lower boiling and melting points than similar carboxylic acids. For example, acetic acid boils at 118 °C, whereas acetyl chloride boils at 51 °C. Like most carbonyl compounds, infrared spectroscopy reveals a band near 1750 cm−1.COA of Formula: C3H3ClO3

《An incisive optical recognition of monohydrogen phosphate by a fluorescein-based chemodosimeter》 was written by Asthana, Sharad Kumar; Pandey, Abha; Kumar, Ajit; Upadhyay, K. K.. COA of Formula: C3H3ClO3 And the article was included in New Journal of Chemistry in 2020. The article conveys some information:

Numerous methods for the determination of phosphates (H2PO4-, HPO42-, PO43-, PPi) are described in the literature. However, the design of optical probes which are able to recognize specifically monohydrogen phosphate (MHP) ions, i.e. HPO42-, has been rarely considered. We herein devised an incisive chemodosimeter (FLH) for detecting HPO42- over other phosphates successfully. In the experiment, the researchers used Methyl 2-chloro-2-oxoacetate(cas: 5781-53-3COA of Formula: C3H3ClO3)

Methyl 2-chloro-2-oxoacetate(cas: 5781-53-3) belongs to acyl chlorides. Lacking the ability to form hydrogen bonds, acyl chlorides have lower boiling and melting points than similar carboxylic acids. For example, acetic acid boils at 118 °C, whereas acetyl chloride boils at 51 °C. Like most carbonyl compounds, infrared spectroscopy reveals a band near 1750 cm−1.COA of Formula: C3H3ClO3

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

Zhao, Shizhen’s team published research in Bioorganic & Medicinal Chemistry in 2021 | CAS: 5781-53-3

Methyl 2-chloro-2-oxoacetate(cas: 5781-53-3) belongs to acyl chlorides. In the laboratory, acyl chlorides are generally prepared by treating carboxylic acids with thionyl chloride (SOCl2). The reaction is catalyzed by dimethylformamide and other additives.Quality Control of Methyl 2-chloro-2-oxoacetate

Zhao, Shizhen; Li, Xinping; Wang, Le; Peng, Wenjing; Ye, Wenling; Li, Weiguo; Wang, Yan-Dong; Chen, Wei-Dong published their research in Bioorganic & Medicinal Chemistry in 2021. The article was titled 《Design, synthesis and evaluation of 1-benzyl-1H-imidazole-5-carboxamide derivatives as potent TGR5 agonists》.Quality Control of Methyl 2-chloro-2-oxoacetate The article contains the following contents:

A series of novel 1-benzyl-1H-imidazole-5-carboxamides I [R1 = 4-methylanilino, 4-fluoro-N-methyl-anilino, 4-phenylpiperazin-1-yl, etc.] and II [R2 = H, 2-Cl, 2,4-di-F, etc.] were designed, synthesized and evaluated in-vitro and in-vivo. The most potent compounds II [R2 = 2,4-di-Cl, 2,5-di-Cl] exhibited excellent agonistic activities against hTGR5, which was superior to those of the reference drugs INT-777 and LCA. In addition, compounds II [R2 = 2,4-di-Cl, 2,5-di-Cl] exhibited good selectivity against FXR and presented significant glucose-lowering effects in-vivo. Compound II [R2 = 2,4-di-Cl] stimulated GLP-1 secretion by activating of TGR5.Methyl 2-chloro-2-oxoacetate(cas: 5781-53-3Quality Control of Methyl 2-chloro-2-oxoacetate) was used in this study.

Methyl 2-chloro-2-oxoacetate(cas: 5781-53-3) belongs to acyl chlorides. In the laboratory, acyl chlorides are generally prepared by treating carboxylic acids with thionyl chloride (SOCl2). The reaction is catalyzed by dimethylformamide and other additives.Quality Control of Methyl 2-chloro-2-oxoacetate

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

Ciccone, Lidia’s team published research in Pharmaceutical Chemistry Journal in 2022 | CAS: 622-95-7

1-(Bromomethyl)-4-chlorobenzene(cas: 622-95-7) may be used to synthesize 1-(4-chlorobenzyl)-2-(pyrrolidin-1-yl-methyl)-1H-benzimidazole dihydrochloride.HPLC of Formula: 622-95-7 It can be synthesized by reacting 4-chlorobenzyl alcohol with bromodimethylsulfonium bromide (BDMS) It can also be synthesized by refluxing a mixture of 4-chlorobenzaldehyde, chlorotrimethylsilane, 1,1,3,3-tetramethyldisiloxane and lithium bromide.

In 2022,Ciccone, Lidia; Nencetti, Susanna; Camodeca, Caterina; Ortore, Gabriella; Cuffaro, Doretta; Socci, Simone; Orlandini, Elisabetta published an article in Pharmaceutical Chemistry Journal. The title of the article was 《Synthesis and Evaluation of Monoaryl Derivatives as Transthyretin Fibril Formation Inhibitors》.HPLC of Formula: 622-95-7 The author mentioned the following in the article:

Here, the synthesis of new 2-((benzyloxy)imino)acetic, -propanoic and -butanoic acid derivatives, RCH2ON=C(R1)C(O)OH (R = 2-chlorophenyl, 4-methoxyphenyl, 2,4-dichlorophenyl, etc.; R1 = H, Me, Et) results of their turbidimetric UV assay and the docking study of new monoaryl compounds were reported. The obtained results suggest that, for this class of compounds, (i) the chlorine atom in ortho position on the aromatic ring is the best substituent; (ii) the linker inversion still allows the interaction with thyroxine binding sites; and (iii) the steric hindrance in R1 position is detrimental for the activity. The results came from multiple reactions, including the reaction of 1-(Bromomethyl)-4-chlorobenzene(cas: 622-95-7HPLC of Formula: 622-95-7)

1-(Bromomethyl)-4-chlorobenzene(cas: 622-95-7) may be used to synthesize 1-(4-chlorobenzyl)-2-(pyrrolidin-1-yl-methyl)-1H-benzimidazole dihydrochloride.HPLC of Formula: 622-95-7 It can be synthesized by reacting 4-chlorobenzyl alcohol with bromodimethylsulfonium bromide (BDMS) It can also be synthesized by refluxing a mixture of 4-chlorobenzaldehyde, chlorotrimethylsilane, 1,1,3,3-tetramethyldisiloxane and lithium bromide.

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

Markushyna, Yevheniia’s team published research in ACS Organic & Inorganic Au in 2022 | CAS: 98-60-2

4-Chlorobenzenesulfonyl chloride(cas: 98-60-2) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties.COA of Formula: C6H4Cl2O2S Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.

COA of Formula: C6H4Cl2O2SIn 2022 ,《Synthesis of Sulfonyl Chlorides from Aryldiazonium Salts Mediated by a Heterogeneous Potassium Poly(heptazine imide) Photocatalyst》 appeared in ACS Organic & Inorganic Au. The author of the article were Markushyna, Yevheniia; Antonietti, Markus; Savateev, Aleksandr. The article conveys some information:

A heterogeneous transition metal-free material, a type of carbon nitride photocatalyst, potassium poly(heptazine imide), was employed to produce sulfonyl chlorides from arenediazonium salts under mild conditions (visible light irradiation, room temperature) with 50-95% yields. The method was suitable for the synthesis of both electron rich and electron deficient compounds and it showed high tolerance toward different functional groups (halides, ester, nitro, cyano groups). Thus, a sustainable photocatalytic alternative to the Meerwein chlorosulfonylation reaction was offered. The experimental process involved the reaction of 4-Chlorobenzenesulfonyl chloride(cas: 98-60-2COA of Formula: C6H4Cl2O2S)

4-Chlorobenzenesulfonyl chloride(cas: 98-60-2) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties.COA of Formula: C6H4Cl2O2S Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.

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