O-ethyl benzoylthiocarbamate

Base Information

Chemical Name:O-ethyl benzoylthiocarbamate
CAS No.:6958-78-7
Molecular Formula:C10H11 N O2 S
Molecular Weight:209.269
Hs Code.:
NSC Number:64888
DSSTox Substance ID:DTXSID60364352
Nikkaji Number:J839.458J

Synonyms:O-ethyl benzoylthiocarbamate;6958-78-7;NSC64888;Enamine_005095;NCIOpen2_003090;O-ethyl benzoylcarbamothioate;N-(ethoxymethanethioyl)benzamide;SCHEMBL15400292;DTXSID60364352;N-[Ethoxy(thiocarbonyl)]benzamide;HMS1408H13;NSC-64888;AKOS001046176;IDI1_007682;benzamido-methanethioic acid O-ethyl ester;Z56871891

Suppliers and Price of O-ethyl benzoylthiocarbamate

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 5 raw suppliers

Chemical Property of O-ethyl benzoylthiocarbamate

Chemical Property:

Density:1.201g/cm³
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:209.05104977
Heavy Atom Count:14
Complexity:212

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=S)NC(=O)C1=CC=CC=C1

Technology Process of O-ethyl benzoylthiocarbamate

There total 8 articles about O-ethyl benzoylthiocarbamate 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: 75.0%

: 64-17-5
ethanol

: 540-72-7
sodium thiocyanide

: 98-88-4
benzoyl chloride

: 6958-78-7
O-ethyl N-benzoylthiocarbamidate

Guidance literature:: sodium thiocyanide; benzoyl chloride; In acetone; at 0 ℃;

ethanol; In acetone; at 20 ℃;

Reference yield:

: 532-55-8
Benzoyl isothiocyanate

: 41368-63-2
sodium derivative of diethyl (hydroxymethyl)phosphonate

: 6958-78-7
O-ethyl N-benzoylthiocarbamidate

: 55-21-0,27208-38-4
benzamide

: diethyl <(benzoyloxy)methyl>phosphonate

Guidance literature:: With benzyl chloride; Yield given. Multistep reaction. Yields of byproduct given; 1) benzene, r.t., 3.5 h, then 35-40 deg C, 1.5 h, 2) benzene, r.t., overnight, then 30-40 deg C, 7 h;