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

Base Information

Chemical Name:N-(4-Bromophenyl)-4-[(dimethylsulfamoyl)amino]benzamide
CAS No.:90234-05-2
Molecular Formula:C₁₅H₁₆BrN₃O₃S
Molecular Weight:398.28
Hs Code.:
ChEMBL ID:CHEMBL132980
DSSTox Substance ID:DTXSID60536830
Wikidata:Q82411614

Synonyms:90234-05-2;CHEMBL132980;N-(4-Bromophenyl)-4-[(dimethylsulfamoyl)amino]benzamide;SCHEMBL10806752;DTXSID60536830;YOQKQNORJMZTJX-UHFFFAOYSA-N;4'-bromo-4-[(dimethylaminosulfonyl)amino]benzanilide

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

Supply Marketing:

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

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Chemical Property of N-(4-Bromophenyl)-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:397.00958
Heavy Atom Count:23
Complexity:491

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

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

There total 4 articles about N-(4-Bromophenyl)-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:

: 59280-03-4
N-(4'-bromophenyl)-4-nitrobenzamide

: 90234-05-2
4'-bromo-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

: 90234-05-2
4'-bromo-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

Reference yield:

: 106-40-1
4-bromo-aniline

: 90234-05-2
4'-bromo-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