2-Thiazolamine, 4-(4-bromophenyl)-N-(4-(2-(4-chlorophenyl)-4-thiazolyl)phenyl)-

Base Information

Chemical Name:2-Thiazolamine, 4-(4-bromophenyl)-N-(4-(2-(4-chlorophenyl)-4-thiazolyl)phenyl)-
CAS No.:68173-72-8
Molecular Formula:C24H15BrClN3S2
Molecular Weight:524.883
Hs Code.:
DSSTox Substance ID:DTXSID10218356
Wikidata:Q83095224
Mol file:68173-72-8.mol

Synonyms:BRN 1182843;68173-72-8;2-Thiazolamine, 4-(4-bromophenyl)-N-(4-(2-(4-chlorophenyl)-4-thiazolyl)phenyl)-;4-(4-Bromophenyl)-N-(4-(2-(4-chlorophenyl)-4-thiazolyl)phenyl)-2-thiazolamine;4-(4-bromophenyl)-N-[4-[2-(4-chlorophenyl)-1,3-thiazol-4-yl]phenyl]-1,3-thiazol-2-amine;4-(4-bromophenyl)-N-{4-[2-(4-chlorophenyl)-1,3-thiazol-4-yl]phenyl}-1,3-thiazol-2-amine;C24H15BrClN3S2;DTXSID10218356;FPJRKHFGUOPTMC-UHFFFAOYSA-N;C24-H15-Br-Cl-N3-S2;LS-150597;AR-009/42290040

Suppliers and Price of 2-Thiazolamine, 4-(4-bromophenyl)-N-(4-(2-(4-chlorophenyl)-4-thiazolyl)phenyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-Thiazolamine, 4-(4-bromophenyl)-N-(4-(2-(4-chlorophenyl)-4-thiazolyl)phenyl)-

Chemical Property:

Vapor Pressure:1.55E-18mmHg at 25°C
Boiling Point:683.5°C at 760 mmHg
Flash Point:367.2°C
PSA：94.29000
Density:1.521g/cm³
LogP:8.83310
XLogP3:8.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:522.95793
Heavy Atom Count:31
Complexity:563

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C2=CSC(=N2)C3=CC=C(C=C3)Cl)NC4=NC(=CS4)C5=CC=C(C=C5)Br

Technology Process of 2-Thiazolamine, 4-(4-bromophenyl)-N-(4-(2-(4-chlorophenyl)-4-thiazolyl)phenyl)-

There total 4 articles about 2-Thiazolamine, 4-(4-bromophenyl)-N-(4-(2-(4-chlorophenyl)-4-thiazolyl)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:

: 2631-71-2
4-aminophenacyl chloride

: 68173-72-8
N-(4-(p-Bromphenyl)-2-thiazolyl)-p-(2-(p-chlorphenyl)-4-thiazolyl)anilin

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / Heating

2: (i) PhCOCl, acetone, (ii) /BRN= 993346/, (iii) aq. NaOH

3: ethanol / Heating

In ethanol;

Reference yield:

: 2521-24-6
4-chlorothiobenzamide

: 68173-72-8
N-(4-(p-Bromphenyl)-2-thiazolyl)-p-(2-(p-chlorphenyl)-4-thiazolyl)anilin

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / Heating

2: (i) PhCOCl, acetone, (ii) /BRN= 993346/, (iii) aq. NaOH

3: ethanol / Heating

In ethanol;

Reference yield:

: 54883-32-8
4-[2-(4-chloro-phenyl)-thiazol-4-yl]-aniline

: 68173-72-8
N-(4-(p-Bromphenyl)-2-thiazolyl)-p-(2-(p-chlorphenyl)-4-thiazolyl)anilin

Guidance literature:: Multi-step reaction with 2 steps

1: (i) PhCOCl, acetone, (ii) /BRN= 993346/, (iii) aq. NaOH

2: ethanol / Heating

In ethanol;