4-Chloro-N-(2-chlorophenyl)benzenecarbothioamide

Base Information

Chemical Name:4-Chloro-N-(2-chlorophenyl)benzenecarbothioamide
CAS No.:91813-43-3
Molecular Formula:C13H9Cl2NS
Molecular Weight:282.193
Hs Code.:
DSSTox Substance ID:DTXSID901238873

Synonyms:4-Chloro-N-(2-chlorophenyl)benzenecarbothioamide;DTXSID901238873;91813-43-3

Suppliers and Price of 4-Chloro-N-(2-chlorophenyl)benzenecarbothioamide

Supply Marketing:

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

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Chemical Property of 4-Chloro-N-(2-chlorophenyl)benzenecarbothioamide

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:280.9832759
Heavy Atom Count:17
Complexity:264

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)NC(=S)C2=CC=C(C=C2)Cl)Cl

Technology Process of 4-Chloro-N-(2-chlorophenyl)benzenecarbothioamide

There total 3 articles about 4-Chloro-N-(2-chlorophenyl)benzenecarbothioamide 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: 79.7%

: 49747-48-0
N-(2-chlorophenyl)-4-chlorophenylamide

: 91813-43-3
N-(2-chlorophenyl)-4-chlorophenylthioamide

Guidance literature:: With Lawessons reagent; In 1,2-dichloro-benzene; at 80 ℃; for 6h; Reflux;

Reference yield:

: 95-51-2
o-chloroaniline

: 91813-43-3
N-(2-chlorophenyl)-4-chlorophenylthioamide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 2 h / Reflux

2: Lawessons reagent / 1,2-dichloro-benzene / 6 h / 80 °C / Reflux

With Lawessons reagent; pyridine; In 1,2-dichloro-benzene;

Reference yield:

: 122-01-0
4-chloro-benzoyl chloride

: 91813-43-3
N-(2-chlorophenyl)-4-chlorophenylthioamide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 2 h / Reflux

2: Lawessons reagent / 1,2-dichloro-benzene / 6 h / 80 °C / Reflux

With Lawessons reagent; pyridine; In 1,2-dichloro-benzene;