4-Amino-N-(4-phenyl-1,3-thiazol-2-yl)benzenesulfonamide

Base Information

Chemical Name:4-Amino-N-(4-phenyl-1,3-thiazol-2-yl)benzenesulfonamide
CAS No.:37615-03-5
Molecular Formula:C15H13 N3 O2 S2
Molecular Weight:0
Hs Code.:2935009090
NSC Number:23574
DSSTox Substance ID:DTXSID10191054
Wikidata:Q83063540
Mol file:37615-03-5.mol

Synonyms:37615-03-5;NSC23574;4-Amino-N-(4-phenyl-1,3-thiazol-2-yl)benzenesulfonamide;Benzenesulfonamide, 4-amino-N-(4-phenyl-2-thiazolyl)-;NSC 23574;Oprea1_691867;DTXSID10191054;NSC-23574;4-amino-N-(4-phenylthiazol-2-yl)benzenesulfonamide

Suppliers and Price of 4-Amino-N-(4-phenyl-1,3-thiazol-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 5 raw suppliers

Chemical Property of 4-Amino-N-(4-phenyl-1,3-thiazol-2-yl)benzenesulfonamide

Chemical Property:

Vapor Pressure:2.23E-13mmHg at 25°C
Boiling Point:578.5°Cat760mmHg
Flash Point:303.6°C
PSA：121.70000
Density:1.448g/cm³
LogP:4.92810
XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:331.04491901
Heavy Atom Count:22
Complexity:452

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CSC(=N2)NS(=O)(=O)C3=CC=C(C=C3)N

Technology Process of 4-Amino-N-(4-phenyl-1,3-thiazol-2-yl)benzenesulfonamide

There total 4 articles about 4-Amino-N-(4-phenyl-1,3-thiazol-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: 56.0%

: 77925-44-1
N-acetyl-sulfanilic acid-(4-phenyl-thiazol-2-ylamide)

: 37615-03-5
sulfanilic acid-(4-phenyl-thiazol-2-ylamide)

Guidance literature:: With sodium hydroxide; for 1h; Heating;
DOI:10.1080/00021369.1981.10864637

Reference yield:

: 121-60-8
p-acetylaminobenzenesulfonyl chloride

: 37615-03-5
sulfanilic acid-(4-phenyl-thiazol-2-ylamide)

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / pyridine / 1 h / Heating

2: 56 percent / 10percent NaOH / 1 h / Heating

With pyridine; sodium hydroxide;
DOI:10.1080/00021369.1981.10864637