N-(4-Chlorophenyl)-4-[(dimethylsulfamoyl)amino]benzamide

Base Information

Chemical Name:N-(4-Chlorophenyl)-4-[(dimethylsulfamoyl)amino]benzamide
CAS No.:90233-88-8
Molecular Formula:C15H16ClN3O3S
Molecular Weight:353.829
Hs Code.:
ChEMBL ID:CHEMBL334442
DSSTox Substance ID:DTXSID50536844
Wikidata:Q82411634

Synonyms:90233-88-8;CHEMBL334442;SCHEMBL10811299;DTXSID50536844;N-(4-Chlorophenyl)-4-[(dimethylsulfamoyl)amino]benzamide;GIPQOWIPVGHBAK-UHFFFAOYSA-N;4'-chloro-4-[(dimethylaminosulfonyl)amino]benzanilide

Suppliers and Price of N-(4-Chlorophenyl)-4-[(dimethylsulfamoyl)amino]benzamide

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 0 raw suppliers

Chemical Property of N-(4-Chlorophenyl)-4-[(dimethylsulfamoyl)amino]benzamide

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:353.0600902
Heavy Atom Count:23
Complexity:491

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)S(=O)(=O)NC1=CC=C(C=C1)C(=O)NC2=CC=C(C=C2)Cl

Technology Process of N-(4-Chlorophenyl)-4-[(dimethylsulfamoyl)amino]benzamide

There total 4 articles about N-(4-Chlorophenyl)-4-[(dimethylsulfamoyl)amino]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:

: 349422-01-1
ethyl 4-<(dimethylsulfamoyl)amino>benzoate

: 90233-88-8
4'-chloro-4-[(dimethylaminosulfonyl)amino]benzanilide

Guidance literature:: Multi-step reaction with 3 steps

1: 10percent NaOH / 0.25 h / 70 °C

2: SOCl₂ / 0.17 h / Heating

3: Et₃N / CH₂Cl₂ / 0.17 h / Ambient temperature

With sodium hydroxide; thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1021/jm00153a018

Reference yield:

: 94-09-7
p-aminoethylbenzoate

: 90233-88-8
4'-chloro-4-[(dimethylaminosulfonyl)amino]benzanilide

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / 16 h / Ambient temperature

2: 10percent NaOH / 0.25 h / 70 °C

3: SOCl₂ / 0.17 h / Heating

4: Et₃N / CH₂Cl₂ / 0.17 h / Ambient temperature

With pyridine; sodium hydroxide; thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1021/jm00153a018

Reference yield:

: 90250-68-3
4-<(dimethylsulfamoyl)amino>benzoic acid

: 90233-88-8
4'-chloro-4-[(dimethylaminosulfonyl)amino]benzanilide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 0.17 h / Heating

2: Et₃N / CH₂Cl₂ / 0.17 h / Ambient temperature

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1021/jm00153a018