Sulfone, p-aminophenyl p-(2-thiazolylamino)phenyl

Base Information

Chemical Name:Sulfone, p-aminophenyl p-(2-thiazolylamino)phenyl
CAS No.:73927-11-4
Molecular Formula:C₁₅H₁₃N₃O₂S₂
Molecular Weight:331.419
Hs Code.:
DSSTox Substance ID:DTXSID10224538
Nikkaji Number:J90.673E
Wikidata:Q83103136
Mol file:73927-11-4.mol

Synonyms:BRN 0295975;Sulfone, p-aminophenyl p-(2-thiazolylamino)phenyl;73927-11-4;p-Amino-p'-(2-thiazolylamino)diphenylsulfone;p-Aminophenyl p-(2-thiazolylamino)phenyl sulfone;4-27-00-04584 (Beilstein Handbook Reference);DTXSID10224538;C15-H13-N3-O2-S2;LS-147957;p-Aminophenyl[p-(2-thiazolylamino)phenyl] sulfone;2-Thiazolamine, N-[4-[(4-aminophenyl)sulfonyl]phenyl]-

Suppliers and Price of Sulfone, p-aminophenyl p-(2-thiazolylamino)phenyl

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 2 raw suppliers

Chemical Property of Sulfone, p-aminophenyl p-(2-thiazolylamino)phenyl

Chemical Property:

Vapor Pressure:3.42E-13mmHg at 25°C
Boiling Point:574.3°C at 760 mmHg
Flash Point:301.1°C
PSA：121.70000
Density:1.448g/cm³
LogP:5.03670
XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:331.04491901
Heavy Atom Count:22
Complexity:450

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)NC3=NC=CS3

Technology Process of Sulfone, p-aminophenyl p-(2-thiazolylamino)phenyl

There total 3 articles about Sulfone, p-aminophenyl p-(2-thiazolylamino)phenyl 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:

: 874509-08-7
[4-(4-nitro-benzenesulfonyl)-phenyl]-thiazol-2-yl-amine

: 73927-11-4
(4-amino-phenyl)-[4-(thiazol-2-ylamino)-phenyl]-sulfone

Guidance literature:: With acetic acid; tin(ll) chloride;
DOI:10.1021/ja01200a025

Reference yield:

: 1948-92-1
4-(4-nitrophenylsulfonyl)aniline

: 73927-11-4
(4-amino-phenyl)-[4-(thiazol-2-ylamino)-phenyl]-sulfone

Guidance literature:: Multi-step reaction with 2 steps

2: SnCl₂; acetic acid

With acetic acid; tin(ll) chloride;
DOI:10.1021/ja01200a025

Reference yield:

: 1775-37-7
N-[4-(4-Nitro-benzenesulfonyl)-phenyl]-acetamide

: 73927-11-4
(4-amino-phenyl)-[4-(thiazol-2-ylamino)-phenyl]-sulfone

Guidance literature:: Multi-step reaction with 3 steps

1: aqueous hydrochloric acid

3: SnCl₂; acetic acid

With hydrogenchloride; acetic acid; tin(ll) chloride;
DOI:10.1021/ja01200a025