Ethenamine, 2-phenyl-

Base Information

Chemical Name:Ethenamine, 2-phenyl-
CAS No.:5694-20-2
Molecular Formula:C8H9N
Molecular Weight:119.166
Hs Code.:
DSSTox Substance ID:DTXSID00276445

Synonyms:aminostyrene;Ethenamine, 2-phenyl-;(2-phenylvinyl)amine;5694-20-2;N-(benzylidene)methylamine;DTXSID00276445;UWRZIZXBOLBCON-UHFFFAOYSA-N

Suppliers and Price of Ethenamine, 2-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 3 raw suppliers

Chemical Property of Ethenamine, 2-phenyl-

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:119.073499291
Heavy Atom Count:9
Complexity:90.7

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=CN

Technology Process of Ethenamine, 2-phenyl-

There total 6 articles about Ethenamine, 2-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: 95.0%

: 102-96-5
(2-nitroethenyl)benzene

: 5694-20-2
N-benzylidenemethylamine

Guidance literature:: With sodium tetrahydroborate; In water; at 45 ℃; for 0.25h;
DOI:10.1002/aoc.3258

Reference yield: 88.0%

: 16722-99-9
β-azidostyrene

: 5694-20-2
N-benzylidenemethylamine

Guidance literature:: With Ba(BH₂S₃)2; In tetrahydrofuran; at 20 ℃;
DOI:10.1080/10426500008076533

Reference yield:

: 104-55-2
3-phenyl-propenal

: 5694-20-2
N-benzylidenemethylamine

Guidance literature:: With glucose dehydrogenase; L-alanin; D-glucose; L-alanine dehydrogenase; amine transaminase; ammonium chloride; sodium hydroxide; In dimethyl sulfoxide; at 37 ℃; for 22h; pH=8.2; Darkness; Enzymatic reaction;
DOI:10.1002/adsc.201301148