4-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide

Base Information

Chemical Name:4-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide
CAS No.:90233-62-8
Molecular Formula:C15H17N3O3S
Molecular Weight:319.384
Hs Code.:
ChEMBL ID:CHEMBL133092
DSSTox Substance ID:DTXSID80536812
Wikidata:Q82411584

Synonyms:90233-62-8;4-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide;CHEMBL133092;SCHEMBL10803589;DTXSID80536812;ZHJIQZOKHAPZRF-UHFFFAOYSA-N;4-[(dimethylaminosulfonyl)amino]benzanilide

Suppliers and Price of 4-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 4-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:319.09906259
Heavy Atom Count:22
Complexity:459

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=CC=C2

Technology Process of 4-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide

There total 5 articles about 4-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide 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:

: methanol-dichloromethane

: 782-45-6
4-amino-benzoic acid anilide

: 13360-57-1
dimethylamino sulfonyl chloride

: 90233-62-8
4-[(dimethylaminosulfonyl)amino]benzanilide

Guidance literature:: With sodium hydroxide; In pyridine;

Reference yield:

: 3460-11-5
4-nitrobenzanilide

: 90233-62-8
4-[(dimethylaminosulfonyl)amino]benzanilide

Guidance literature:: Multi-step reaction with 2 steps

1: Sn, 6 N HCl / tetrahydrofuran / 1 h / 50 °C

2: pyridine / 1.5 h / 60 °C

With pyridine; hydrogenchloride; tin; In tetrahydrofuran;
DOI:10.1021/jm00153a018

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 90233-62-8
4-[(dimethylaminosulfonyl)amino]benzanilide

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N / CH₂Cl₂ / 0.08 h / Ambient temperature

2: Sn, 6 N HCl / tetrahydrofuran / 1 h / 50 °C

3: pyridine / 1.5 h / 60 °C

With pyridine; hydrogenchloride; tin; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00153a018