29671-30-5

Basic information

• Product Name: 2-Chlorocaproic acid
• Synonyms: 2-Chlorocaproic acid;2-Chlorohexanoic acid
• CAS NO: 29671-30-5
• Molecular Formula: C₆H₁₁ClO₂
• Molecular Weight: 150.60334
• Mol File: 29671-30-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Chlorocaproic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chlorocaproic acid(29671-30-5)
• EPA Substance Registry System: 2-Chlorocaproic acid(29671-30-5)

Safety Data

• Hazardous Substances Data: 29671-30-5(Hazardous Substances Data)

Upstream product

• 63216-75-1 2-chlorohexan-1-ol 
• 534-59-8 n-butylmalonic acid 
• 142-62-1 hexanoic acid 
• 91674-65-6 2-Chlor-capronohydroxamsaeure-chlorid 
• 15250-08-5 2-chloro-1-hydroperoxy-cyclohexanol 
• 109-49-9 5-Hexen-2-one 
• 13898-47-0 hypochloric acid 
• 592-41-6 1-hexene 

Downstream Products

• 85153-52-2 ethyl ester of the 2-chlorocapronic acid 
• 59011-98-2 2-[4-(4-Trifluoromethyl-phenoxy)-phenoxy]-hexanoic acid 
• 93568-81-1 5-butyl-2-(2-chloro-benzylamino)-thiazol-4-one 
• 93568-82-2 5-butyl-2-(4-chloro-benzylamino)-thiazol-4-one 
• 94064-30-9 5-butyl-2-(3-methyl-benzylamino)-thiazol-4-one 
• 92648-21-0 5-butyl-2-(4-methyl-benzylamino)-thiazol-4-one 
• 93568-66-2 2-(4-bromo-benzylamino)-5-butyl-thiazol-4-one 
• 97020-39-8 5-butyl-2-(2,5-dimethyl-benzylamino)-thiazol-4-one 
• 97020-40-1 5-butyl-2-(3,4-dimethyl-benzylamino)-thiazol-4-one 
• 97020-38-7 5-butyl-2-(2,4-dimethyl-benzylamino)-thiazol-4-one 
• 92292-50-7 2-benzylamino-5-butyl-thiazol-4-one 
• 14925-60-1 methyl α-chlorohexanoate 
• 132586-63-1 2-Chloro-hexanoic acid 4-{5-[4-(2-chloro-hexanoyloxy)-phenyl]-pyrimidin-2-yl}-phenyl ester 
• 114351-31-4 2-Chloro-hexanoic acid {2-[2-(thiazol-2-ylcarbamoyl)-acetyl]-6-trifluoromethyl-phenyl}-amide 

Relevant articles and documents

α-Chlorination of Carboxylic Acids Using Trichloroisocyanuric Acid

Carboxylic acids are chlorinated in the a position by heating with trichloroisocyanuric acid after formation of a small amount of the acid chloride using phosphorus trichloride.

-

-

Ring opening of fluoroepoxyalcohols by nucleophiles

The fluoroepoxyalcohols formed by diastereoselective or asymmetric epoxidation of o-fluoro secondary allylic alcohols can be transformed into various α-substituted ketols by nucleophiles.Key Words: fluoroepoxyalcohols / nucleophiles / α-substituted ketols