Urea, 1-(2-chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-3-nitroso-

Base Information

Chemical Name:Urea, 1-(2-chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-3-nitroso-
CAS No.:13909-28-9
Molecular Formula:C₁₂H₁₅ClN₄O₃
Molecular Weight:298.729
Hs Code.:2924299090
NSC Number:95963
DSSTox Substance ID:DTXSID90160905
Wikidata:Q83029246
ChEMBL ID:CHEMBL273416
Mol file:13909-28-9.mol

Synonyms:13909-28-9;Urea, 1-(2-chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-3-nitroso-;4-[[2-chloroethyl(nitroso)carbamoyl]amino]-N,N-dimethylbenzamide;Benzamide,N-dimethyl;Urea, 1-(2-chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-1-nitroso-;Urea, 1-(2-chloroethyl)-3-[p-(dimethylcarbamoyl)phenyl]-1-nitroso-;NSC95963;NSC 95963;BRN 2892387;CHEMBL273416;DTXSID90160905;1-(2-Chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-3-nitrosourea;NSC-95963;Benzamide, 4-((((2-chloroethyl)nitrosoamino)carbonyl)amino)-N,N-dimethyl

Suppliers and Price of Urea, 1-(2-chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-3-nitroso-

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 5 raw suppliers

Chemical Property of Urea, 1-(2-chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-3-nitroso-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：82.08000
Density:1.31g/cm³
LogP:2.21550
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:298.0832680
Heavy Atom Count:20
Complexity:357

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN(C)C(=O)C1=CC=C(C=C1)NC(=O)N(CCCl)N=O

Technology Process of Urea, 1-(2-chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-3-nitroso-

There total 2 articles about Urea, 1-(2-chloroethyl)-3-(p-(dimethylcarbamoyl)phenyl)-3-nitroso- 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:

: 16106-38-0
4-aminobenzoyl chloride

: 13909-28-9
4-({[(2-chloroethyl)nitrosoamino]carbonyl}amino)-N,N-dimethyl-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: benzene

2: CHCl₃

3: NaNO₂, HCO₂H

With formic acid; sodium nitrite; In chloroform; benzene;
DOI:10.1021/jm00324a026