N-(benzylideneamino)-4-phenyl-1,3-thiazol-2-amine

Base Information

Chemical Name:N-(benzylideneamino)-4-phenyl-1,3-thiazol-2-amine
CAS No.:4216-52-8
Molecular Formula:C16H13N3S
Molecular Weight:233.27
Hs Code.:
DSSTox Substance ID:DTXSID50350486
Mol file:4216-52-8.mol

Synonyms:N-(benzylideneamino)-4-phenyl-1,3-thiazol-2-amine;DTXSID50350486;AKOS030694475;benzaldehyde 4-phenyl-2-thiazolylhydrazone

Suppliers and Price of N-(benzylideneamino)-4-phenyl-1,3-thiazol-2-amine

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 N-(benzylideneamino)-4-phenyl-1,3-thiazol-2-amine

Chemical Property:

Vapor Pressure:7.56E-09mmHg at 25°C
Boiling Point:465.6°Cat760mmHg
Flash Point:235.4°C
Density:1.19g/cm³
XLogP3:4.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:279.08301860
Heavy Atom Count:20
Complexity:309

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=NNC2=NC(=CS2)C3=CC=CC=C3

Technology Process of N-(benzylideneamino)-4-phenyl-1,3-thiazol-2-amine

There total 3 articles about N-(benzylideneamino)-4-phenyl-1,3-thiazol-2-amine 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:

: 6315-23-7
3-(1H-benzimidazol-2-yl)-propionic acid ethyl ester

: 4216-52-8
[2-(1H-benzoimidazol-2-yl)-ethyl]-carbamic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol; N₂H₄+H₂O

2: HCl

With hydrogenchloride; ethanol; hydrazine hydrate;