N-(Benzenecarbothioyl)-4-chlorobenzamide

Base Information

Chemical Name:N-(Benzenecarbothioyl)-4-chlorobenzamide
CAS No.:52810-03-4
Molecular Formula:C14H10ClNOS
Molecular Weight:275.75300
Hs Code.:
DSSTox Substance ID:DTXSID90523930
Wikidata:Q82390377
Mol file:52810-03-4.mol

Synonyms:52810-03-4;N-(Benzenecarbothioyl)-4-chlorobenzamide;DTXSID90523930

Suppliers and Price of N-(Benzenecarbothioyl)-4-chlorobenzamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-(Benzenecarbothioyl)-4-chlorobenzamide

Chemical Property:

PSA：64.68000
LogP:4.02030
XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:275.0171628
Heavy Atom Count:18
Complexity:307

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of N-(Benzenecarbothioyl)-4-chlorobenzamide

There total 4 articles about N-(Benzenecarbothioyl)-4-chlorobenzamide 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:

: 4-Chloro-N-[1-dimethylamino-1-phenyl-meth-(E)-ylidene]-benzamide

: 52810-03-4
4-Chloro-N-thiobenzoyl-benzamide

Guidance literature:: With hydrogen sulfide; In acetic acid; for 0.5h; Yield given; Ambient temperature;
DOI:10.1055/s-1984-31030

Reference yield:

: 19429-87-9
α,α-diethoxy-N,N-dimethylbenzenemethanamine

: 52810-03-4
4-Chloro-N-thiobenzoyl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1 h / 120 °C

2: H₂S / acetic acid / 0.5 h / Ambient temperature

With hydrogen sulfide; In acetic acid;
DOI:10.1055/s-1984-31030

Reference yield:

: 619-56-7
4-chlorobenzamide

: 52810-03-4
4-Chloro-N-thiobenzoyl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1 h / 120 °C

2: H₂S / acetic acid / 0.5 h / Ambient temperature

With hydrogen sulfide; In acetic acid;
DOI:10.1055/s-1984-31030