Benzenecarbothioamide, N-[(1R)-1-phenylethyl]-

Base Information

Chemical Name:Benzenecarbothioamide, N-[(1R)-1-phenylethyl]-
CAS No.:86022-50-6
Molecular Formula:C15H15NS
Molecular Weight:241.357
Hs Code.:
DSSTox Substance ID:DTXSID40350733
Wikidata:Q82126823

Synonyms:Benzenecarbothioamide, N-[(1R)-1-phenylethyl]-;86022-50-6;DTXSID40350733

Suppliers and Price of Benzenecarbothioamide, N-[(1R)-1-phenylethyl]-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of Benzenecarbothioamide, N-[(1R)-1-phenylethyl]-

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:241.09252066
Heavy Atom Count:17
Complexity:239

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)NC(=S)C2=CC=CC=C2
Isomeric SMILES:C[C@H](C1=CC=CC=C1)NC(=S)C2=CC=CC=C2

Technology Process of Benzenecarbothioamide, N-[(1R)-1-phenylethyl]-

There total 1 articles about Benzenecarbothioamide, N-[(1R)-1-phenylethyl]- 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: 77.0%

: 20826-48-6
(R)-N-(1-phenylethyl)benzamide

: 86022-50-6
N-<(R)-1-Phenylethyl>thiobenzamide

Guidance literature:: With Lawessons reagent; In toluene;
DOI:10.1016/0957-4166(96)00406-5

Reference yield: 93.0%

: 35660-94-7
(E)-2-methylbut-2-enoyl chloride

: 86022-50-6
N-<(R)-1-Phenylethyl>thiobenzamide

: 155512-53-1
N-<(R)-1-Phenylethyl>-N-tigloylthiobenzamide

Guidance literature:: With triethylamine; In benzene; for 2h;
DOI:10.1021/jo00090a034

Reference yield:

: 86022-50-6
N-<(R)-1-Phenylethyl>thiobenzamide

: 4,5-Dimethyl-1-phenyl-2-<(R)-1-phenylethyl>-6-thia-2-azabicyclo<2.2.0>hexan-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / Et₃N / benzene / 2 h

2: 0.08 h / -78 °C

With triethylamine; In benzene;
DOI:10.1021/jo00090a034