76076-40-9

Basic information

• Product Name: (+)-2-methyl-2-phenyl-3-butenal
• Synonyms: (+)-2-methyl-2-phenyl-3-butenal
• CAS NO: 76076-40-9
• Molecular Weight: 160.216
• Mol File: 76076-40-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (+)-2-methyl-2-phenyl-3-butenal(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-2-methyl-2-phenyl-3-butenal(76076-40-9)
• EPA Substance Registry System: (+)-2-methyl-2-phenyl-3-butenal(76076-40-9)

Safety Data

• Hazardous Substances Data: 76076-40-9(Hazardous Substances Data)

Upstream product

• 98-83-9 isopropenylbenzene 
• 22433-39-2 1-methyl-1-phenylallene 
• 17343-73-6 (2,2-dibromo-1-methylcyclopropyl)benzene 
• 704-80-3 (E)-3-phenyl-2-butenoic acid 
• 76076-41-0 (R)-1-Cyanomethyl-2-methyl-1-((E)-3-phenyl-but-2-enyl)-pyrrolidinium; chloride 
• 76076-39-6 (R)-2-((S)-2-Benzyloxymethyl-pyrrolidin-1-yl)-3-methyl-3-phenyl-pent-4-enenitrile 

Downstream Products

• 6006-75-3 (-)-2-methyl-2-phenyl-1-butanol 

Relevant articles and documents

Construction of All-Carbon Chiral Quaternary Centers through CuI-Catalyzed Enantioselective Reductive Hydroxymethylation of 1,1-Disubstituted Allenes with CO2

A catalytic enantioselective construction of all-carbon chiral quaternary centers through reductive hydroxymethylation of 1,1-disubstituted allenes with CO2 has been developed. In the presence of a copper/Mandyphos catalyst, CO2 is t

ASYMMETRIC INDUCTION IN THE SIGMATROPIC REARRANGEMENT VIA CHIRAL AMMONIUM YLIDES

The asymmetric sigmatropic rearrangements of the chiral ammonium chlorides (E)-(3a,b) were achieved upon treatment with t-BuOK followed by acidic hydrolysis of the aminonitriles (5a,b) obtained to give (R)-(+)-2-methyl-2-phenyl-3-butenal (6).The rea