Benzenecarbothioamide, N-(2-methylphenyl)-

Base Information

Chemical Name:Benzenecarbothioamide, N-(2-methylphenyl)-
CAS No.:26060-28-6
Molecular Formula:C14H13NS
Molecular Weight:227.33
Hs Code.:
DSSTox Substance ID:DTXSID40355602
Nikkaji Number:J1.855.849A
Wikidata:Q82134610

Synonyms:N-(o-Tolyl)benzothioamide;26060-28-6;Benzenecarbothioamide, N-(2-methylphenyl)-;SCHEMBL15468323;DTXSID40355602;AKOS000507818;SB80134

Suppliers and Price of Benzenecarbothioamide, N-(2-methylphenyl)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Benzenecarbothioamide, N-(2-methylphenyl)-

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:227.07687059
Heavy Atom Count:16
Complexity:233

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=CC=C1NC(=S)C2=CC=CC=C2

Technology Process of Benzenecarbothioamide, N-(2-methylphenyl)-

There total 8 articles about Benzenecarbothioamide, N-(2-methylphenyl)- 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: 78.0%

: 103-82-2
phenylacetic acid

: 88-72-2
1-methyl-2-nitrobenzene

: 26060-28-6
N-(2-methylphenyl)thiobenzamide

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; sulfur; In neat (no solvent); at 120 ℃; for 6h; Inert atmosphere;
DOI:10.1039/c9ob01751h

Reference yield: 72.0%

: 150-60-7
dibenzyl disulphide

: 95-53-4
o-toluidine

: 26060-28-6
N-(2-methylphenyl)thiobenzamide

Guidance literature:: With N-methylcyclohexylamine; sulfur; dimethyl sulfoxide; at 100 ℃; for 16h; Inert atmosphere;
DOI:10.1002/adsc.201801695

Reference yield: 32.0%

: 4949-88-6
N-benzoyl-N'-(2-methylphenyl)thiourea

: 584-70-3
N-benzoyl-2-methylaniline

: 26060-28-6
N-(2-methylphenyl)thiobenzamide

Guidance literature:: With iodine-alumina; In neat (no solvent); at 100 ℃; for 0.333333h; Overall yield = 85 %; Microwave irradiation;
DOI:10.1039/c4nj02021a