S-(2-acetophenyl) benzothioate

Base Information

Chemical Name:S-(2-acetophenyl) benzothioate
CAS No.:130826-24-3
Molecular Formula:C₁₅H₁₂O₂S
Molecular Weight:256.325
Hs Code.:

Synonyms:S-(2-acetophenyl) benzothioate

Suppliers and Price of S-(2-acetophenyl) benzothioate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of S-(2-acetophenyl) benzothioate

Chemical Property:

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of S-(2-acetophenyl) benzothioate

There total 3 articles about S-(2-acetophenyl) benzothioate 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: 96.0%

: 26824-02-2
1-(2-mercaptophenyl)ethan-1-one

: 98-88-4
benzoyl chloride

: 130826-24-3
S-(2-acetophenyl) benzothioate

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.5012/bkcs.2011.32.4.1383

Reference yield:

: 934-87-2
S-phenyl thioacetate

: 130826-24-3
S-(2-acetophenyl) benzothioate

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / AlCl₃ / CS₂ / 0.5 h / 120 - 125 °C

2: 87 percent / 10percent NaOH

With sodium hydroxide; aluminium trichloride; In carbon disulfide;

Reference yield:

: 147-93-3
Thiosalicylic acid

: 130826-24-3
S-(2-acetophenyl) benzothioate

Guidance literature:: Multi-step reaction with 2 steps

1: 1,2-dimethoxyethane / 1 h / -15 - 0 °C

2: triethylamine / dichloromethane / 0.5 h / 0 °C

With triethylamine; In 1,2-dimethoxyethane; dichloromethane;
DOI:10.5012/bkcs.2011.32.4.1383