Singh, V. P. et al. published their research in Oxidation Communications in 1997 | CAS: 14070-51-0

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) 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. 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).Application of 14070-51-0

Kinetic and mechanistic consideration of the degradative oxidation of substituted mandelic acids by N-chlorosaccharin was written by Singh, V. P.;Khan, M. U.;Chauhan, D. B. S.;Verma, J. K.. And the article was included in Oxidation Communications in 1997.Application of 14070-51-0 This article mentions the following:

Kinetic data for the oxidation of p-chloro- and p-bromomandelic acids with N-chlorosaccharin (I) in aqueous AcOH were determined The reaction rate is a direct function of both [oxidant] and [substrate] in the lower concentration region, but tends toward zero order at higher substrate concentrations A retarding trend of H+ ions, solvent composition and saccharin on the system was observed The redox process proceeds via formation of an activated transition complex (1:1) between substrate and postulated HOCl reacting species of I, which slowly disintegrates into products. The oxidation products were confirmed, and a probable mechanism was suggested which was consistent with all observed kinetic results. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0Application of 14070-51-0).

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) 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. 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).Application of 14070-51-0

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

Zhan, Bei-Bei et al. published their research in Chemical Communications (Cambridge, United Kingdom) in 2016 | CAS: 36157-41-2

2,5-Dichlorothiophene-3-carboxylic acid (cas: 36157-41-2) 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. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.HPLC of Formula: 36157-41-2

Nickel-catalyzed ortho-halogenation of unactivated (hetero)aryl C-H bonds with lithium halides using a removable auxiliary was written by Zhan, Bei-Bei;Liu, Yan-Hua;Hu, Fang;Shi, Bing-Feng. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2016.HPLC of Formula: 36157-41-2 This article mentions the following:

The first example of Ni-catalyzed halogenation of (hetero)aryl C-H bonds with lithium halides (LiX, X = Br, I, Cl) using PIP as a removable directing group was reported. This protocol provided an efficient access to ortho-halogenated (hetero)arenes with operational simplicity, good functional group tolerance and large-scale synthesis. In the experiment, the researchers used many compounds, for example, 2,5-Dichlorothiophene-3-carboxylic acid (cas: 36157-41-2HPLC of Formula: 36157-41-2).

2,5-Dichlorothiophene-3-carboxylic acid (cas: 36157-41-2) 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. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.HPLC of Formula: 36157-41-2

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

Saripalli, Harikrishna Ramaprasad et al. published their research in International Journal of Pharma and Bio Sciences in 2021 | CAS: 3386-33-2

1-Chlorooctadecane (cas: 3386-33-2) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. 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.COA of Formula: C18H37Cl

GC-MS analysis of bioactive components in the methanolic extract of graviola (Gishta) seeds and their pharmacological activities was written by Saripalli, Harikrishna Ramaprasad;Dixit, Prasanna Kumar. And the article was included in International Journal of Pharma and Bio Sciences in 2021.COA of Formula: C18H37Cl This article mentions the following:

Bioactive substances are the leading-edge mols. in both the pharmaceutical and nutraceutical industries. Recently, bioactive compounds are gaining much importance for their enhanced resistance to numerous diseases and in boosting people′s health by both traditional and modern ways of administration. In traditional medicine, many plants have provided valuable clues for being used as potential antiparasitic, antimalarial, leishmanicidal, anti-tumor, fungicidal, and antibacterial compounds Still, several plants are yet to be screened for their abilities to stand forth as medicinal plants. Locally, Graviola (Gishta) fruits are being used for dietary purposes and traditional medicinal purposes, but their beneficial effects have never been attributed to the presence of active bio compounds Hence, the present investigation was undertaken to study Gas Chromatog.-Mass Spectrometry (GC-MS) anal. of methanolic extracts of Graviola seeds. GC-MS anal. method was employed with specific conditions such as Ion source temp 200°C, Interface temp 240°C, Scan range 40 – 1000 m/z, MS start time 5(min), MS end time 35 (min), Ionization EI (-70ev), Scan speed 2000. The methanolic extracts of Graviola seeds exhibited the presence of seventy types of bioactive compounds The foremost important compounds identified are 1H-Cyclopenta [l, 3] cyclopropa [l, 2] benzene, octa hydro-7-methyl-3-methylene-4-(1-Me ethyl) -, [3aS-(3a. alpha.,3b. beta., 4. beta., 7. alpha.,7 aS*)]-Bicyclo [4. 4. 0] dec-1-ene, 2-isopropyl-5-methyl-9-methylene-. gamma.-Muurolene. tetracosane, phytol and squalene. In an exceeding mass spectral view, each of the compounds has been identified based on their retention time and percentage of peak area(s). Analytes with high peak areas showed various pharmacol. properties such as antibacterial, antifungal, anticancer, etc. which provided exptl. evidence for its traditional medicinal claim. The spectra of phytochem. constituents found in the seed extracts signify the potential of the Graviola plant as a source of therapeutic agent(s) and may provide leads in the ongoing search for a novel phytotherapeutic agent. In the experiment, the researchers used many compounds, for example, 1-Chlorooctadecane (cas: 3386-33-2COA of Formula: C18H37Cl).

1-Chlorooctadecane (cas: 3386-33-2) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. 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.COA of Formula: C18H37Cl

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

Babaeva, L. G. et al. published their research in Reaktsionnaya Sposobnost Organicheskikh Soedinenii in 1974 | CAS: 5335-05-7

Chloromethyl benzoate (cas: 5335-05-7) 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 readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Related Products of 5335-05-7

Kinetics of hydrolysis for esters with a variable alcoholic part. III. Alkaline hydrolysis of esters of p-nitrobenzoic acid in water was written by Babaeva, L. G.;Bogatkov, S. V.;Kruglikova, R. I.;Unkovskii, B. V.;Unkovskii, B. V.. And the article was included in Reaktsionnaya Sposobnost Organicheskikh Soedinenii in 1974.Related Products of 5335-05-7 This article mentions the following:

The saponification kinetics of p-O2NC6H4CO2R (R = PhCH2CH2, PhCH2, MeOCH2CH2, Me, ClCH2CH2, Ph, ClCH2) were determined at 25° in H2O. Correlation parameters for the dependence of the rate constants on the inductive and steric substituent constants of the alc. part of the mol. were determined The correlation parameters were independent of the acidic part of the esters. In the experiment, the researchers used many compounds, for example, Chloromethyl benzoate (cas: 5335-05-7Related Products of 5335-05-7).

Chloromethyl benzoate (cas: 5335-05-7) 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 readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Related Products of 5335-05-7

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

Frank, Kristine E. et al. published their research in Journal of Organic Chemistry in 2000 | CAS: 18437-66-6

tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) 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.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Category: chlorides-buliding-blocks

Cyclizations of Substituted Benzylidene-3-alkenylamines: Synthesis of the Tricyclic Core of the Martinellines was written by Frank, Kristine E.;Aube, Jeffrey. And the article was included in Journal of Organic Chemistry in 2000.Category: chlorides-buliding-blocks This article mentions the following:

The martinellines are natural products that possess both interesting biol. activity and chem. structure. During the investigation of a hetero Diels-Alder route to these mols., alternate Lewis acid-dependent cyclizations of (2′-amino-N’-tert-butoxycarbonyl-5′-chlorobenzylidene)-3-butenylamine were observed The reaction of a variety of imines with TMSOTf or TiCl4 led to the formation of different heterocycles including iminodibenzo[b,f][1,5]diazocines, hexahydropyrido[1,2-c]quinazolin-6-ones, tetrahydropyrrolo[1,2-c]quinazolin-5-ones, 2-arylpiperidines, and 2-arylpyrrolidines. Tetrahydropyrrolo[1,2-c]quinazolin-5-one I, obtained via this new methodol., was used as an intermediate in the synthesis of the tricyclic ring system (II) of the martinellines. In the experiment, the researchers used many compounds, for example, tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6Category: chlorides-buliding-blocks).

tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) 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.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Category: chlorides-buliding-blocks

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

Chu, Senlin et al. published their research in BMC Pulmonary Medicine in 2022 | CAS: 61-73-4

3,7-Bis(dimethylamino)phenothiazin-5-ium chloride (cas: 61-73-4) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.COA of Formula: C16H18ClN3S

Comparative study of the effect of preoperative hookwire and methylene blue localization techniques on post-operative hospital stay and complications in thoracoscopic pulmonary nodule surgery was written by Chu, Senlin;Wei, Ning;Lu, Dong;Chai, Jie;Liu, Shun;Lv, Weifu. And the article was included in BMC Pulmonary Medicine in 2022.COA of Formula: C16H18ClN3S This article mentions the following:

Abstract: Background: Direct localization of small and deep pulmonary nodules before thoracoscopic surgery using the hookwire or methylene blue techniques has been recently attempted for better surgical outcomes. In this study, we compare the outcomes of the above two techniques. Methods: Two hundred and nineteen patients undergoing 135 hookwire and 151 methylene blue techniques in our University Hospital between July 2020 and Jan. 2022 were compared for localization and hospitalization durations, and the complication risk. Other confounders included patients′ age, gender, localization position, nodules location, count, diameter, and depth. Results: After adjustment of all predictors, the methylene blue technique was associated with a significant 0.6-min (parameter estimate (PE) = -0.568, p value = 0.0173) and an 0.7-day shorter localization and hospitalization time (PE = -0.713, p value = < 0.0001) as compared to using the hookwire technique. The hookwire technique was significantly associated with 5 times the risk of developing a post-localization complication (Adjusted Odds Ratio (Adj OR) = 4.52, 95% CI 1.53-13.33) and 3.6 times the risk of developing a pneumothorax (Adj OR = 3.57, 95% CI 1.1-11.62) as compared to adopting the methylene blue technique. Conclusions: Compared to the hook wire technique, the methylene blue technique offers a shorter procedure and hospitalization stay, as well as a safer post-operative experience. In the experiment, the researchers used many compounds, for example, 3,7-Bis(dimethylamino)phenothiazin-5-ium chloride (cas: 61-73-4COA of Formula: C16H18ClN3S).

3,7-Bis(dimethylamino)phenothiazin-5-ium chloride (cas: 61-73-4) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.COA of Formula: C16H18ClN3S

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

Guruge, Keerthi S. et al. published their research in Chemosphere in 2021 | CAS: 101-20-2

1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea (cas: 101-20-2) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Electric Literature of C13H9Cl3N2O

The association between antimicrobials and the antimicrobial-resistant phenotypes and resistance genes of Escherichia coli isolated from hospital wastewaters and adjacent surface waters in Sri Lanka was written by Guruge, Keerthi S.;Tamamura, Yukino A.;Goswami, Prasun;Tanoue, Rumi;Jinadasa, K. B. S. N.;Nomiyama, Kei;Ohura, Takeshi;Kunisue, Tatsuya;Tanabe, Shinsuke;Akiba, Masato. And the article was included in Chemosphere in 2021.Electric Literature of C13H9Cl3N2O This article mentions the following:

The presence of antimicrobials, antimicrobial-resistant bacteria (ARB), and the associated antimicrobial resistance genes (ARGs) in the environment is a global health concern. In this study, the concentrations of 25 antimicrobials, the resistance of Escherichia coli (E. coli) strains in response to the selection pressure imposed by 15 antimicrobials, and enrichment of 20 ARGs in E. coli isolated from hospital wastewaters and surface waters were investigated from 2016 to 2018. In hospital wastewaters, clarithromycin was detected at the highest concentration followed by sulfamethoxazole and sulfapyridine. Approx. 80% of the E. coli isolates were resistant, while 14% of the isolates exhibited intermediate resistance against the tested antimicrobial agents. Approx. 61% of the examined isolates were categorized as multidrug-resistant bacteria. The overall abundance of phenotypes that were resistant toward drugs was in the following order: β-lactams, tetracycline, quinolones, sulfamethoxazole/trimethoprim, aminoglycosides, and chloramphenicol. The data showed that the E. coli isolates frequently harbored blaTEM, blaCTX-M, tetA, qnrS, and sul2. These results indicated that personal care products were significantly associated with the presence of several resistant phenotypes and resistance genes, implying their role in co-association with multidrug resistance. Statistical anal. also indicated a disparity specific to the site, treatment, and year in the data describing the prevalence of ARB and ARGs and their release into downstream waters. This study provides novel insights into the abundance of antimicrobial, ARB and ARGs in Sri Lanka, and could further offer invaluable information that can be integrated into global antimicrobial resistance databases. 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 stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Electric Literature of C13H9Cl3N2O

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

Kumar, Kishan et al. published their research in Journal of the Indian Chemical Society in 1974 | CAS: 3438-16-2

5-Chloro-2-methoxybenzoic acid (cas: 3438-16-2) 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.Recommanded Product: 3438-16-2

Mannich reaction. N-[2-Hydroxy-3 (or 5 or 6)-substituted] benzyl glycines was written by Kumar, Kishan;Pandey, N. D.;Mehrotra, J. K.. And the article was included in Journal of the Indian Chemical Society in 1974.Recommanded Product: 3438-16-2 This article mentions the following:

Mannich reaction of glycine and HCHO with substituted phenols gave 35-65% I (R1 = H; R2, R3, R4 = H, Me, Cl, CO2H), which were methylated with Me2SO to give 50-96% of the corresponding I (R1 = Me). Thus, glycine, HCHO, and PhOH in NaOAc and HOAc gave 38.67% I (R1-R4 = H), which was methylated with Me2SO4 in NaOH at 80° to give 60.97% Me2SO4 (R1 = Me, R2-R4 =H). In the experiment, the researchers used many compounds, for example, 5-Chloro-2-methoxybenzoic acid (cas: 3438-16-2Recommanded Product: 3438-16-2).

5-Chloro-2-methoxybenzoic acid (cas: 3438-16-2) 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.Recommanded Product: 3438-16-2

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

Xu, Xun-Hui et al. published their research in Chemical Science in 2022 | CAS: 76-83-5

(Chloromethanetriyl)tribenzene (cas: 76-83-5) 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.Quality Control of (Chloromethanetriyl)tribenzene

Precise fabrication of porous polymer frameworks using rigid polyisocyanides as building blocks: from structural regulation to efficient iodine capture was written by Xu, Xun-Hui;Li, Yan-Xiang;Zhou, Li;Liu, Na;Wu, Zong-Quan. And the article was included in Chemical Science in 2022.Quality Control of (Chloromethanetriyl)tribenzene This article mentions the following:

Porous materials have recently attracted much attention owing to their fascinating structures and broad applications. Moreover, exploring novel porous polymers affording the efficient capture of iodine is of significant interest. In contrast to the reported porous polymers fabricated with small mol. blocks, we herein report the preparation of porous polymer frameworks using rigid polyisocyanides as building blocks. First, tetrahedral four-arm star polyisocyanides with predictable mol. weight and low dispersity were synthesized; the chain-ends of the rigid polyisocyanide blocks were then crosslinked, yielding well-defined porous organic frameworks with a designed pore size and narrow distribution. Polymers of appropriate pore size were observed to efficiently capture radioactive iodine in both aqueous and vapor phases. More than 98% of iodine could be captured within 1 min from a saturated aqueous solution (capacity of up to 3.2 g g-1), and an adsorption capacity of up to 574 wt% of iodine in vapor was measured within 4 h. Moreover, the polymers could be recovered and recycled for iodine capture for at least six times, while maintaining high performance. In the experiment, the researchers used many compounds, for example, (Chloromethanetriyl)tribenzene (cas: 76-83-5Quality Control of (Chloromethanetriyl)tribenzene).

(Chloromethanetriyl)tribenzene (cas: 76-83-5) 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.Quality Control of (Chloromethanetriyl)tribenzene

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

Feng, Chengliang et al. published their research in Journal of Chemical Research in 2013 | CAS: 18437-66-6

tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Recommanded Product: tert-Butyl (4-chlorophenyl)carbamate

Iron(III) triflate as a highly efficient, recyclable and green catalyst for the N-Boc protection of amines was written by Feng, Chengliang;Chu, Ningning;Zhang, Shuguang;Cai, Jin;Chen, Junqing;Hu, Huayou;Ji, Min. And the article was included in Journal of Chemical Research in 2013.Recommanded Product: tert-Butyl (4-chlorophenyl)carbamate This article mentions the following:

Iron(III) triflate was used as an efficient catalyst for N-t-butoxycarbonylation of amines with di-t-Bu dicarbonate under solvent-free conditions at room temperature Various aliphatic, aromatic, heterocyclic amines and aminols were protected as their corresponding mono-carbamates in excellent yields and short reaction times. Only two of the 23 monocarbamates were new. No competitive side reactions such as isocyanate, urea, nor N,N-di-Boc formation were observed The reported method is mild and has the advantages of low cost, chemoselectivity and, because no solvent is used and the catalyst can be recycled, it is classifiable as a green procedure. In the experiment, the researchers used many compounds, for example, tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6Recommanded Product: tert-Butyl (4-chlorophenyl)carbamate).

tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Recommanded Product: tert-Butyl (4-chlorophenyl)carbamate

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