3-(4-Phenyl-thiazol-2-yl)-phenylamine

Base Information

Chemical Name:3-(4-Phenyl-thiazol-2-yl)-phenylamine
CAS No.:134811-95-3
Molecular Formula:C₁₅H₁₂N₂S
Molecular Weight:252.34
Hs Code.:
DSSTox Substance ID:DTXSID501293108
Mol file:134811-95-3.mol

Synonyms:3-(4-Phenyl-thiazol-2-yl)-phenylamine;134811-95-3;3-(4-phenyl-1,3-thiazol-2-yl)aniline;Oprea1_793638;DTXSID501293108;3-(4-Phenyl-2-thiazolyl)benzenamine;3-(4-Phenylthiazol-2-yl)phenylamine;AKOS005082269;1G-444S

Suppliers and Price of 3-(4-Phenyl-thiazol-2-yl)-phenylamine

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 3-(4-Phenyl-thiazol-2-yl)-phenylamine

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:252.07211956
Heavy Atom Count:18
Complexity:265

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 3-(4-Phenyl-thiazol-2-yl)-phenylamine

There total 4 articles about 3-(4-Phenyl-thiazol-2-yl)-phenylamine 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:

: 58202-84-9
N-(3-cyanophenyl)acetamide

: 134811-95-3
2-(3-aminophenyl)-4-phenylthiazole

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / H₂S, Et₃N, pyridine / 6 h / Ambient temperature

2: ethanol / Heating

3: conc. HCl / 2 h / Heating

With pyridine; hydrogenchloride; hydrogen sulfide; triethylamine; In ethanol;
DOI:10.1002/jhet.5570280324

Reference yield:

: 93029-92-6
3-acetylaminothiobenzamide

: 134811-95-3
2-(3-aminophenyl)-4-phenylthiazole

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / Heating

2: conc. HCl / 2 h / Heating

With hydrogenchloride; In ethanol;
DOI:10.1002/jhet.5570280324

Reference yield:

: 2237-30-1
m-cyanoaniline

: 134811-95-3
2-(3-aminophenyl)-4-phenylthiazole

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / gl. acetic acid / 6 h / Heating

2: 96 percent / H₂S, Et₃N, pyridine / 6 h / Ambient temperature

3: ethanol / Heating

4: conc. HCl / 2 h / Heating

With pyridine; hydrogenchloride; hydrogen sulfide; acetic acid; triethylamine; In ethanol;
DOI:10.1002/jhet.5570280324