4-Amino-2-chlorobenzenesulfonamide

Base Information

Chemical Name:4-Amino-2-chlorobenzenesulfonamide
CAS No.:1954-94-5
Molecular Formula:C6H7ClN2O2S
Molecular Weight:206.653
Hs Code.:
DSSTox Substance ID:DTXSID20501584
Wikidata:Q82354048
Mol file:1954-94-5.mol

Synonyms:4-amino-2-chlorobenzenesulfonamide;1954-94-5;4-Amino-2-chlorobenzene-1-sulfonamide;3-Chloro-4-sulphamoylaniline;SCHEMBL1383117;DTXSID20501584;NIDOTDANGJJHPU-UHFFFAOYSA-N;BAA95494;BS-50668;CS-0162699;E76539;EN300-271541

Suppliers and Price of 4-Amino-2-chlorobenzenesulfonamide

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 10 raw suppliers

Chemical Property of 4-Amino-2-chlorobenzenesulfonamide

Chemical Property:

XLogP3:0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:205.9916763
Heavy Atom Count:12
Complexity:249

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C=C1N)Cl)S(=O)(=O)N

Technology Process of 4-Amino-2-chlorobenzenesulfonamide

There total 4 articles about 4-Amino-2-chlorobenzenesulfonamide 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: 71.0%

: 1954-94-5
4-amino-2-chlorobenzenesulfonamide

Guidance literature:

Reference yield:

: 72290-18-7
6-acetylamino-2-chloro-3-sulfamoyl-benzoic acid

: 1954-94-5
4-amino-2-chlorobenzenesulfonamide

Guidance literature:: With hydrogenchloride;
DOI:10.1248/cpb.27.1287

Reference yield:

: 7463-35-6
N-(3-chloro-2-methylphenyl)acetamide

: 1954-94-5
4-amino-2-chlorobenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: (i) ClSO₃H, NaCl, (ii) aq. NH₃

2: KMnO₄

3: aq. HCl

With hydrogenchloride; potassium permanganate;
DOI:10.1248/cpb.27.1287