29671-30-5

Upstream product

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

Downstream Products

• 14925-60-1 methyl α-chlorohexanoate 
• 83119-77-1 2-(2,3-Dichloro-4-methoxy-phenylsulfanyl)-hexanoyl chloride 
• 114351-31-4 2-Chloro-hexanoic acid {2-[2-(thiazol-2-ylcarbamoyl)-acetyl]-6-trifluoromethyl-phenyl}-amide 
• 132586-63-1 2-Chloro-hexanoic acid 4-{5-[4-(2-chloro-hexanoyloxy)-phenyl]-pyrimidin-2-yl}-phenyl ester 
• 92292-50-7 2-benzylamino-5-butyl-thiazol-4-one 
• 97020-38-7 5-butyl-2-(2,4-dimethyl-benzylamino)-thiazol-4-one 
• 97020-40-1 5-butyl-2-(3,4-dimethyl-benzylamino)-thiazol-4-one 
• 97020-39-8 5-butyl-2-(2,5-dimethyl-benzylamino)-thiazol-4-one 
• 93568-66-2 2-(4-bromo-benzylamino)-5-butyl-thiazol-4-one 
• 92648-21-0 5-butyl-2-(4-methyl-benzylamino)-thiazol-4-one 
• 94064-30-9 5-butyl-2-(3-methyl-benzylamino)-thiazol-4-one 
• 93568-82-2 5-butyl-2-(4-chloro-benzylamino)-thiazol-4-one 
• 93568-81-1 5-butyl-2-(2-chloro-benzylamino)-thiazol-4-one 
• 59011-98-2 2-[4-(4-Trifluoromethyl-phenoxy)-phenoxy]-hexanoic acid 

Relevant academic research and scientific papers

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.

Decyclization of chlorocyclohexanone hydroperoxides under the action of ferrous salts

The decomposition of 2-chloro-, 2,2-dichloro-, and 2,6-dichloro-substituted cyclohexanone hydroperoxides on treatment with ferrous chloride and sulfate to give chloro-substituted aliphatic acids was investigated. A method for the synthesis of 2,6,6-trichlorohexanoic and 2,6,7,11-tetrachlorododecane-1,12-dioic acids was elaborated.

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

Asymmetric Transformation of 2-Phenyl- and 2-Chloroalkanoic Acids via Chiral Oxazolines

Asymmetric transformation of racemic 2-phenyl- and 2-chloroalkanoic acids via oxazolines into the corresponding optically active acids was investigated using (S)-phenylalaninol as a chiral auxiliary.The asymmetric transformation was performed by metalatio