(E)-4-(2-(4-Fluorophenyl)ethenyl)benzenamine, N,N-dimethyl-

Base Information

Chemical Name:(E)-4-(2-(4-Fluorophenyl)ethenyl)benzenamine, N,N-dimethyl-
CAS No.:38695-34-0
Molecular Formula:C₁₆H₁₆FN
Molecular Weight:241.308
Hs Code.:
Nikkaji Number:J48.674D
Pharos Ligand ID:Z9BYDVDH11MD
ChEMBL ID:CHEMBL81999
Mol file:38695-34-0.mol

Synonyms:38695-34-0;(E)-4-(2-(4-Fluorophenyl)ethenyl)benzenamine, N,N-dimethyl-;CHEMBL81999;4-[(E)-2-(4-fluorophenyl)ethenyl]-N,N-dimethylaniline;SCHEMBL2951021;SCHEMBL2951023;NNAWDQWHXHKJPH-ONEGZZNKSA-N;4-(Dimethylamino)-4'-fluorostilbene;BDBM50481134;(E)-4-Fluoro-4'-dimethylamino-stilbene;{4-[2-(4-Fluoro-phenyl)-vinyl]-phenyl}-dimethyl-amine;4-(2-(4-fluorophenyl)ethenyl)benzenamine,n,n-dimethyl-;(E)-4-(2-(4-Fluorophenyl)ethenyl)benzenamine, N,N-dimethyl

Suppliers and Price of (E)-4-(2-(4-Fluorophenyl)ethenyl)benzenamine, N,N-dimethyl-

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 (E)-4-(2-(4-Fluorophenyl)ethenyl)benzenamine, N,N-dimethyl-

Chemical Property:

Vapor Pressure:2.02E-05mmHg at 25°C
Melting Point:197 - 198 °C (acetonitrile)
Boiling Point:361.8°C at 760 mmHg
Flash Point:172.6°C
PSA：3.24000
Density:1.123g/cm³
LogP:4.06210
XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:241.126677677
Heavy Atom Count:18
Complexity:258

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C1=CC=C(C=C1)C=CC2=CC=C(C=C2)F
Isomeric SMILES:CN(C)C1=CC=C(C=C1)/C=C/C2=CC=C(C=C2)F

Technology Process of (E)-4-(2-(4-Fluorophenyl)ethenyl)benzenamine, N,N-dimethyl-

There total 11 articles about (E)-4-(2-(4-Fluorophenyl)ethenyl)benzenamine, N,N-dimethyl- 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: 80.0%