4-chloro-N-(phenylcarbamothioyl)benzamide

Base Information

Chemical Name:4-chloro-N-(phenylcarbamothioyl)benzamide
CAS No.:59849-18-2
Molecular Formula:C14H11ClN2OS
Molecular Weight:290.773
Hs Code.:
DSSTox Substance ID:DTXSID00358038
Nikkaji Number:J1.703.477D
Wikidata:Q82138304

Synonyms:4-chloro-N-(phenylcarbamothioyl)benzamide;STK045395;59849-18-2;CBMicro_047085;DTXSID00358038;AKOS003420272;BIM-0047083.P001

Suppliers and Price of 4-chloro-N-(phenylcarbamothioyl)benzamide

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-(phenylcarbamothioyl)benzamide

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:290.0280618
Heavy Atom Count:19
Complexity:323

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 4-chloro-N-(phenylcarbamothioyl)benzamide

There total 5 articles about 4-chloro-N-(phenylcarbamothioyl)benzamide 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: 80.0%

: 62-53-3
aniline

: 16794-67-5
p-chlorobenzoyl isothiocyanate

: 59849-18-2
1-(4-chloro-benzoyl)-3-phenyl-thiourea

Guidance literature:

Reference yield: 12.0%

: 1132-44-1
1-acetyl-3-phenylthiourea

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

: 59849-18-2
1-(4-chloro-benzoyl)-3-phenyl-thiourea

Guidance literature:: In acetone; for 3h; Heating;

Reference yield:

: 74-11-3
para-chlorobenzoic acid

: 59849-18-2
1-(4-chloro-benzoyl)-3-phenyl-thiourea

Guidance literature:: Multi-step reaction with 2 steps

1.1: SOCl₂ / 5.5 h / Heating

2.1: acetone / 0.17 h / 20 °C

2.2: acetone / 0.17 h / Heating

With thionyl chloride; In acetone;
DOI:10.1039/b102029n