(p-Chlorobenzoyl)urea

Base Information

Chemical Name:(p-Chlorobenzoyl)urea
CAS No.:6940-51-8
Molecular Formula:C8H7ClN2O2
Molecular Weight:198.6064
Hs Code.:
NSC Number:60140
DSSTox Substance ID:DTXSID00989225
Nikkaji Number:J2.890.230A
Wikidata:Q82978160

Synonyms:(p-Chlorobenzoyl)urea;Urea, (p-chlorobenzoyl)-;6940-51-8;NSC 60140;BRN 1953483;Benzamide, N-(aminocarbonyl)-4-chloro-;NSC60140;1-(4-Chlorobenzoyl)urea;SCHEMBL9117609;DTXSID00989225;NSC-60140;AKOS013520747;LS-159303;4-Chloro-N-[hydroxy(imino)methyl]benzene-1-carboximidic acid

Suppliers and Price of (p-Chlorobenzoyl)urea

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of (p-Chlorobenzoyl)urea

Chemical Property:

Density:1.393g/cm³
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:198.0196052
Heavy Atom Count:13
Complexity:212

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)NC(=O)N)Cl

Technology Process of (p-Chlorobenzoyl)urea

There total 6 articles about (p-Chlorobenzoyl)urea 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: 86.0%

: 57-13-6
urea

: 74-11-3
para-chlorobenzoic acid

: 6940-51-8
N-carbamoyl-4-chlorobenzamide

Guidance literature:: With pyridine; triphenyl phosphite; In N,N-dimethyl-formamide; at 100 ℃; for 2h;

Reference yield: 39.0%

: C₁₄H₉ClO₂S

: 6940-51-8
N-carbamoyl-4-chlorobenzamide

Guidance literature:: With trimethylsilylazide; copper diacetate; In N,N-dimethyl-formamide; at 80 ℃; for 1h; Molecular sieve; Inert atmosphere;
DOI:10.1021/acs.joc.7b03054

Reference yield:

: 5372-78-1
4-chloro-N-cyanobenzamide

: 6940-51-8
N-carbamoyl-4-chlorobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: PCl₅ / benzene

2: aq. NaOH

With sodium hydroxide; phosphorus pentachloride; In benzene;