70525-38-1

Basic information

• Product Name: (E)-2-(2-phenylprop-1-en-1-yl)pyridine
• Synonyms: (E)-2-(2-phenylprop-1-en-1-yl)pyridine
• CAS NO: 70525-38-1
• Molecular Weight: 195.264
• Mol File: 70525-38-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (E)-2-(2-phenylprop-1-en-1-yl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(2-phenylprop-1-en-1-yl)pyridine(70525-38-1)
• EPA Substance Registry System: (E)-2-(2-phenylprop-1-en-1-yl)pyridine(70525-38-1)

Safety Data

• Hazardous Substances Data: 70525-38-1(Hazardous Substances Data)

Upstream product

• 110-86-1 pyridine 
• 98-85-1 1-Phenylethanol 
• 38700-15-1 triphenyl-(2-pyridylmethyl)phosphonium chloride 
• 109-06-8 α-picoline 
• 585-71-7 (1-bromoethyl)benzne 
• 108-86-1 bromobenzene 
• 52248-74-5 (E)-2-(prop-1-en-1-yl)pyridine 
• 17881-80-0 (2-picolyl)trimethylsilane 
• 1749-19-5 N-(1-phenylethylidene)aniline 

Relevant articles and documents

Aryl-Nickel-Catalyzed Benzylic Dehydrogenation of Electron-Deficient Heteroarenes

This manuscript describes the first practical benzylic dehydrogenation of electron-deficient heteroarenes, including pyridines, pyrazines, pyrimidines, pyridazines, and triazines. This transformation allows for the efficient benzylic oxidation of heteroarenes to afford heterocyclic styrenes by the action of nickel catalysis paired with an unconventional bromothiophene oxidant.

Ruthenium-catalyzed arylation of 2-alkenylpyridines with aryl bromides: Alternative E,Z-selectivity to Mizoroki-Heck reaction

(Chemical Equation Presented) Regio- and stereoselective arylation of 2-alkenylpyridines with aryl bromides is catalyzed by specific Ru(II)-phosphine complexes affording β-arylated (Z)-2-alkenylpyridines, in which the aryl moiety is introduced cis to the

STEREOSPECIFIC SYNTHESIS OF (E)-ALKENYLPYRIDINES VIA α-SILYL CARBANION

(E)-2-Alkenylpyridines were stereospecifically prepared from 2-(trimethylsilylmethyl)pyridine and the corresponding (E)-aldimines of anilines by an analogous reaction to the Peterson reaction.