55847-36-4

Basic information

• Product Name: Ethanethioic acid, S-(2-chloroethyl) ester
• Synonyms: 2-chloroethyl thioacetate;2-Chlor-aethylthioacetat;2-Chlorethylthiolacetat
• CAS NO: 55847-36-4
• Molecular Formula: C4H7ClOS
• Molecular Weight: 138.618
• Mol File: 55847-36-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Ethanethioic acid, S-(2-chloroethyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanethioic acid, S-(2-chloroethyl) ester(55847-36-4)
• EPA Substance Registry System: Ethanethioic acid, S-(2-chloroethyl) ester(55847-36-4)

Safety Data

• Hazardous Substances Data: 55847-36-4(Hazardous Substances Data)

Upstream product

• 17642-74-9 2-methyl-1,3-oxathiolane 

Downstream Products

• 91880-70-5 ω-<β-Chlor-aethylmercapto>-acetophenon 
• 6050-81-3 S-acetylthiocholine chloride 
• 100-38-9 2-(diethylamine)ethanethiol 
• 685-91-6 diethylacetamide 

Relevant articles and documents

KINETICS AND MECHANISM OF HOMOLYTIC TRANSFORMATIONS OF 1,3-OXATHIOLANES IN CARBON TETRACHLORIDE

In carbon tetrachloride in the presence of tert-butyl peroxide at 120-150 deg C 1,3-oxathiolanes are converted into chloroethyl thioacylates.The kinetics were studied and an unbranched radical-chain mechanism for the formation of the chlorothio esters through the formation of 2-chloro-1,3-oxathiolanes is proposed.The controlling stage of the process is the abstraction of a hydrogen atom from the substrate by the trichloromethyl radical.The effect of the nature of the heteroatom and substituent at position 2 of the heterocycle on the reactivity of the substrate was dtermined.