4-(2,2-Diphenylethenyl)pyridine

Base Information

Chemical Name:4-(2,2-Diphenylethenyl)pyridine
CAS No.:15814-97-8
Molecular Formula:C₁₉H₁₅N
Molecular Weight:257.335
Hs Code.:
ChEMBL ID:CHEMBL381194
DSSTox Substance ID:DTXSID001304182
Nikkaji Number:J3.317.753D
Pharos Ligand ID:MYSZR39PKGWJ

Synonyms:4-(2,2-diphenylethenyl)pyridine;4-Pyridylmethylene 35;BDBM8645;CHEMBL381194;SCHEMBL16946606;DTXSID001304182;15814-97-8;PD181608

Suppliers and Price of 4-(2,2-Diphenylethenyl)pyridine

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

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Chemical Property of 4-(2,2-Diphenylethenyl)pyridine

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:257.120449483
Heavy Atom Count:20
Complexity:282

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=CC2=CC=NC=C2)C3=CC=CC=C3

Technology Process of 4-(2,2-Diphenylethenyl)pyridine

There total 3 articles about 4-(2,2-Diphenylethenyl)pyridine 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: 91.0%

: 108-89-4
picoline

: 119-61-9
benzophenone

: 15814-97-8
4-(2,2-diphenylvinyl)pyridine

Guidance literature:: With tris(trimethylsilyl)amine; tetramethylammonium fluoride; In N,N-dimethyl-formamide; at 80 ℃; for 24h; Inert atmosphere; Glovebox; Sealed tube;
DOI:10.1021/acs.orglett.9b00550

Reference yield:

: 91-01-0
1,1-Diphenylmethanol

: 15814-97-8
4-(2,2-diphenylvinyl)pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: benzene / 12 h / Heating

2: K₂CO₃; 18-crown-6 / CH₂Cl₂ / 12 h / Heating

With 18-crown-6 ether; potassium carbonate; In dichloromethane; benzene; 2: Wittig reaction;
DOI:10.1021/jm0492397