4-Amino-N-(6-chloro-1,5-naphthyridin-2-yl)benzenesulfonamide

Base Information

Chemical Name:4-Amino-N-(6-chloro-1,5-naphthyridin-2-yl)benzenesulfonamide
CAS No.:54996-17-7
Molecular Formula:C14H11ClN4O2S
Molecular Weight:334.7807
Hs Code.:
DSSTox Substance ID:DTXSID90203523
Wikidata:Q83076924

Synonyms:4-Amino-N-(6-chloro-1,5-naphthyridin-2-yl)benzenesulfonamide;BRN 0694666;54996-17-7;Benzenesulfonamide, 4-amino-N-(6-chloro-1,5-naphthyridin-2-yl)-;2-(4'-Aminobenzenesulfonamido)-6-chloro-1,5-naphthyridine;5-25-11-00133 (Beilstein Handbook Reference);DTXSID90203523;LS-31233

Suppliers and Price of 4-Amino-N-(6-chloro-1,5-naphthyridin-2-yl)benzenesulfonamide

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 1 raw suppliers

Chemical Property of 4-Amino-N-(6-chloro-1,5-naphthyridin-2-yl)benzenesulfonamide

Chemical Property:

Vapor Pressure:1.91E-13mmHg at 25°C
Boiling Point:580°C at 760 mmHg
Flash Point:304.6°C
Density:1.569g/cm³
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:334.0291245
Heavy Atom Count:22
Complexity:476

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N)S(=O)(=O)NC2=NC3=C(C=C2)N=C(C=C3)Cl

Technology Process of 4-Amino-N-(6-chloro-1,5-naphthyridin-2-yl)benzenesulfonamide

There total 1 articles about 4-Amino-N-(6-chloro-1,5-naphthyridin-2-yl)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: