Ethanethioic acid, S-[4-(chlorocarbonyl)phenyl] ester (9CI)

Base Information

Chemical Name:Ethanethioic acid, S-[4-(chlorocarbonyl)phenyl] ester (9CI)
CAS No.:129018-26-4
Molecular Formula:C9H7ClO2S
Molecular Weight:214.672
Hs Code.:
Mol file:129018-26-4.mol

Synonyms:Ethanethioic acid, S-[4-(chlorocarbonyl)phenyl] ester (9CI)

Suppliers and Price of Ethanethioic acid, S-[4-(chlorocarbonyl)phenyl] ester (9CI)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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price

Total 2 raw suppliers

Chemical Property of Ethanethioic acid, S-[4-(chlorocarbonyl)phenyl] ester (9CI)

Chemical Property:

PSA：59.44000
LogP:2.70420

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

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Hazard Codes:

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Technology Process of Ethanethioic acid, S-[4-(chlorocarbonyl)phenyl] ester (9CI)

There total 3 articles about Ethanethioic acid, S-[4-(chlorocarbonyl)phenyl] ester (9CI) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

: 24197-62-4
S-acetyl-4-mercaptobenzoic acid

: 129018-26-4
thioacetic acid S-(4-chlorocarbonyl-phenyl) ester

Guidance literature:: With oxalyl dichloride; In benzene; for 1h; Heating;
DOI:10.1039/DT9900003375

Reference yield:

: 1074-36-8
4-mercaptobenzoic acid

: 129018-26-4
thioacetic acid S-(4-chlorocarbonyl-phenyl) ester

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / KOH; AcOH

2: SOCl₂ / 1 h / Heating

With potassium hydroxide; thionyl chloride; acetic acid;
DOI:10.1002/chem.200500729

Reference yield:

: 13511-93-8
S-(4-carbomethoxyphenyl) N,N-dimethylthiocarbamate

: 129018-26-4
thioacetic acid S-(4-chlorocarbonyl-phenyl) ester

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / 10percent NaOH / methanol; H₂O / 3 h / Heating

2: 88 percent / pyridine

3: 80 percent / oxalyl chloride / benzene / 1 h / Heating

With pyridine; sodium hydroxide; oxalyl dichloride; In methanol; water; benzene;
DOI:10.1039/DT9900003375