2-Acetamidophenyl thioacetate

Base Information

Chemical Name:2-Acetamidophenyl thioacetate
CAS No.:28045-65-0
Molecular Formula:C10H11 N O2 S
Molecular Weight:209.269
Hs Code.:
DSSTox Substance ID:DTXSID80182318
Wikidata:Q83052981
Mol file:28045-65-0.mol

Synonyms:2-Acetamidophenyl thioacetate;BRN 2838199;USAF AB-14;ACETIC ACID, THIO-, 2-(ACETAMIDOPHENYL) ESTER;28045-65-0;DTXSID80182318

Suppliers and Price of 2-Acetamidophenyl thioacetate

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 4 raw suppliers

Chemical Property of 2-Acetamidophenyl thioacetate

Chemical Property:

Boiling Point:391.4±25.0 °C(Predicted)
PKA:13.12±0.70(Predicted)
PSA：73.91000
Density:1.245g/cm³
LogP:3.02060
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:209.05104977
Heavy Atom Count:14
Complexity:230

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC=CC=C1OC(=S)C

Technology Process of 2-Acetamidophenyl thioacetate

There total 8 articles about 2-Acetamidophenyl thioacetate 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: 68.0%

: 587-65-5
N-chloroacetyl-aniline

: 28045-65-0
2-S-(acetylthio)-N-phenylacetamide

Guidance literature:: With potassium thioacetate; In acetone; at 20 ℃; for 3h;
DOI:10.1039/d1md00187f

Reference yield:

: 62-53-3
aniline

: 28045-65-0
2-S-(acetylthio)-N-phenylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine; chloroacetyl chloride / dichloromethane / 2 h / 0 °C

2: potassium thioacetate / acetone / 3 h / 20 °C

With N-ethyl-N,N-diisopropylamine; chloroacetyl chloride; potassium thioacetate; In dichloromethane; acetone;
DOI:10.1039/d1md00187f