Carbamothioic acid, benzoyl-, S-2-propenyl ester

Base Information

Chemical Name:Carbamothioic acid, benzoyl-, S-2-propenyl ester
CAS No.:41876-77-1
Molecular Formula:C11H11NO2S
Molecular Weight:221.28
Hs Code.:
DSSTox Substance ID:DTXSID801236931

Synonyms:Carbamothioic acid, benzoyl-, S-2-propenyl ester;DTXSID801236931;41876-77-1

Suppliers and Price of Carbamothioic acid, benzoyl-, S-2-propenyl ester

Supply Marketing:

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

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Chemical Property of Carbamothioic acid, benzoyl-, S-2-propenyl ester

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:221.05104977
Heavy Atom Count:15
Complexity:247

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCSC(=O)NC(=O)C1=CC=CC=C1

Technology Process of Carbamothioic acid, benzoyl-, S-2-propenyl ester

There total 3 articles about Carbamothioic acid, benzoyl-, S-2-propenyl ester 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: 83.0%

: 113283-11-7
O-(2-propenyl) N-benzoylmonothiocarbamate

: 41876-77-1
S-(2-propenyl) N-benzoylmonothiocarbamate

Guidance literature:: In benzene; for 9h; Heating;

Reference yield:

: 532-55-8
Benzoyl isothiocyanate

: 41876-77-1
S-(2-propenyl) N-benzoylmonothiocarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / benzene / 96 h / Ambient temperature

2: 83 percent / benzene / 9 h / Heating

In benzene;