N-(4-Bromophenyl)benzenesulfonamide

Base Information

• Chemical Name: N-(4-Bromophenyl)benzenesulfonamide
• CAS No.: 16468-97-6
• Molecular Formula: C12H10 Br N O2 S
• Molecular Weight: 312.187
• Hs Code.: 2935009090
• European Community (EC) Number: 654-099-6
• NSC Number: 159417
• DSSTox Substance ID: DTXSID40303623
• Nikkaji Number: J124.121D
• Wikidata: Q82048996
• Mol file: 16468-97-6.mol

Synonyms:N-(4-Bromophenyl)benzenesulfonamide;16468-97-6;Benzenesulfonamide, N-(4-bromophenyl)-;4'-Bromobenzenesulfonanilide;Benzenesulfonanilide, 4'-bromo-;(4-bromophenyl)(phenylsulfonyl)amine;NSC159417;DTXSID40303623;N-p-bromophenylbenzenesulphonamide;HHLFFQAEABRCOJ-UHFFFAOYSA-N;4-(Difluoromethoxy)phenacylbromide;MFCD00159375;STK056574;AKOS000171746;N-(4-Bromo-phenyl)-benzenesulfonamide;N-(4-Bromophenyl)benzenesulfonamide #;CCG-105190;NSC-159417;CS-0270219;EU-0003126;AE-641/00009022;SR-01000416253;SR-01000416253-1;Z45620033

Chemical Property of N-(4-Bromophenyl)benzenesulfonamide

Chemical Property:

• Boiling Point: 423.1°Cat760mmHg
• Flash Point: 209.7°C
• PSA: 54.55000
• Density: 1.603g/cm³
• LogP: 4.40370
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 310.96156
• Heavy Atom Count: 17
• Complexity: 325

Purity/Quality:

99% ^*data from raw suppliers

4''-Bromo-benzenesulfonanilide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of N-(4-Bromophenyl)benzenesulfonamide

There total 10 articles about N-(4-Bromophenyl)benzenesulfonamide 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: 96.8%

benzenesulfonyl chloride (98-09-9) + 4-bromo-aniline (106-40-1) → N-(4-bromophenyl)benzenesulfonamide (16468-97-6)

Guidance literature:

In pyridine;

Reference yield: 93.0%

benzenesulfonyl chloride (98-09-9) + para-nitrophenyl bromide (586-78-7) → N-(4-bromophenyl)benzenesulfonamide (16468-97-6)

Guidance literature:

With iron; In water; for 0.833333h;

Reference yield: 92.0%

sodium benzenesulfonate (873-55-2) + 4-bromo-aniline (106-40-1) → N-(4-bromophenyl)benzenesulfonamide (16468-97-6)

Guidance literature:

With iodine; In 1,2-dichloro-ethane; at 25 ℃; for 24h;

DOI:10.1002/adsc.201400801

upstream raw materials:

benzenesulfonyl chloride

4-bromo-aniline

benzenesulfonamide

1,4-bromoiodobenzene

Downstream raw materials:

N-(4-bromophenyl)-N-methyl-benzenesulfonamide