1461649-10-4

Basic information

• Product Name: (R,E)-1-methyl-4-(4-phenylbut-3-en-2-yl)benzene
• Synonyms: (R,E)-1-methyl-4-(4-phenylbut-3-en-2-yl)benzene
• CAS NO: 1461649-10-4
• Molecular Weight: 222.33
• Mol File: 1461649-10-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R,E)-1-methyl-4-(4-phenylbut-3-en-2-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (R,E)-1-methyl-4-(4-phenylbut-3-en-2-yl)benzene(1461649-10-4)
• EPA Substance Registry System: (R,E)-1-methyl-4-(4-phenylbut-3-en-2-yl)benzene(1461649-10-4)

Safety Data

• Hazardous Substances Data: 1461649-10-4(Hazardous Substances Data)

Upstream product

• 16939-57-4 (E)-buta-1,3-dienylbenzene 
• 195062-57-8 p-tolylboronic pinacol ester 
• 67826-86-2 (E)-diisobutyl(styryl)aluminum 
• 159755-12-1 1-(1-bromoethyl)-4-methylbenzene 
• 17488-65-2 4-phenylbut-3-en-2-ol 
• 5720-05-8 4-methylphenylboronic acid 
• 81176-43-4 (S)-trans-4-phenyl-3-buten-2-ol 

Relevant articles and documents

Enantioselective Synthesis of Functionalized Arenes by Nickel-Catalyzed Site-Selective Hydroarylation of 1,3-Dienes with Aryl Boronates

A catalytic method for the site-selective and enantioselective synthesis of functionalized arenes by the intermolecular hydroarylation of terminal and internal 1,3-dienes with aryl pinacolato boronates is reported. The reactions are promoted by 5.0 mol %

Pd-Catalyzed stereospecific allyl-aryl coupling of allylic alcohols with arylboronic acids

An efficient method for Pd-catalyzed stereospecific allyl-aryl coupling of allylic alcohols with arylboronic acids has been described. The reactions proceeded smoothly in the presence of Pd2(dba)3· CHCl3 and racemic BINAP