1342313-03-4

Basic information

• Product Name: (R)-2-methyl-2-phenyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal
• Synonyms: (R)-2-methyl-2-phenyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal
• CAS NO: 1342313-03-4
• Molecular Weight: 370.432
• Mol File: 1342313-03-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-2-methyl-2-phenyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-methyl-2-phenyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal(1342313-03-4)
• EPA Substance Registry System: (R)-2-methyl-2-phenyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal(1342313-03-4)

Safety Data

• Hazardous Substances Data: 1342313-03-4(Hazardous Substances Data)

Upstream product

• 34713-70-7 2-Phenylpropanal 
• 1154397-00-8 1-phenyl-5-(vinylsulfonyl)-1H-tetrazole 
• 1153358-38-3 5-((2-chloroethyl)thio)-1-phenyl-1H-tetrazole 

Downstream Products

• 67679-06-5 (R)-(-)-2-methyl-2-phenyl-4-pentenylaldehyde 
• 1342313-30-7 (R)-5-(3-(1,3-dioxolan-2-yl)-3-phenylbutylsulfonyl)-1-phenyl-1H-tetrazole 

Relevant articles and documents

Enantioselective organocatalytic formal allylation of α-branched aldehydes

Heteroarylvinyl sulfone 1 has been successfully used as a new sulfonyl Michael acceptor in aminocatalytic reactions with branched aldehydes. Subsequent one-pot Julia-Kocienski olefination allows the challenging preparation of enantiomerically pure α-allylated aldehydes bearing C-α quaternary carbons.