1201829-81-3

Basic information

• Product Name: (R)-3-methyl-4,4-bis(phenylsulfonyl)butanal
• Synonyms: (R)-3-methyl-4,4-bis(phenylsulfonyl)butanal
• CAS NO: 1201829-81-3
• Molecular Weight: 366.459
• Mol File: 1201829-81-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (R)-3-methyl-4,4-bis(phenylsulfonyl)butanal(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-methyl-4,4-bis(phenylsulfonyl)butanal(1201829-81-3)
• EPA Substance Registry System: (R)-3-methyl-4,4-bis(phenylsulfonyl)butanal(1201829-81-3)

Safety Data

• Hazardous Substances Data: 1201829-81-3(Hazardous Substances Data)

Upstream product

• 123-73-9 trans-Crotonaldehyde 
• 3406-02-8 bis(phenylsulfonyl)methane 
• 123-73-9 crotonaldehyde 

Downstream Products

• 1186231-90-2 (R)-3-methyl-4,4-bis(phenylsulfonyl)butan-1-ol 
• 1201829-92-6 (R)-3-methyl-4,4-bis(phenylsulfonyl)butanoic acid 
• 1201829-96-0 (R)-2-(2-methyl-3,3-bis(phenylsulfonyl)propyl)-1,3-dioxane 
• 109685-43-0 (R)-4,4,4-trifluoro-3-methylbutyl benzoate 
• 1331743-73-7 (3R)-3-methyl-4-(methylsulfanyl)-4-(phenylsulfonyl)butyl benzoate 
• 1331743-71-5 (3R)-3-methyl-4-(methylsulfanyl)-4-(phenylsulfonyl)butan-1-ol 
• 1331743-69-1 (3R)-3-methyl-4-(methylsulfanyl)-4-(phenylsulfonyl)butan-1-ol tert-butyldimethylsilyl ether 
• 1331743-67-9 (R)-3-methyl-4-(phenylsulfonyl)butan-1-ol tert-butyldimethylsilyl ether 
• 1331743-65-7 (R)-3-methyl-4,4-bis(phenylsulfonyl)butan-1-ol tert-butyldimethylsilyl ether 

Relevant articles and documents

A theoretical and experimental study of the effects of silyl substituents in enantioselective reactions catalyzed by diphenylprolinol silyl ether

The effect of silyl substituents in diphenylprolinol silyl ether catalysts was investigated. Mechanistically, reactions catalyzed by diphenylprolinol silyl ether can be categorized into three types: two that involve an iminium ion intermediate, such as fo

Formal highly enantioselective organocatalytic addition of alkyl anions to α,β-unsaturated aldehydes: Application to the synthesis of isotope-enantiomers

A practical and powerful methodology that constitutes an organocatalytic alternative for organometallic 1,4-additions was developed. In a vial, bis(phenylsulfonyl)methane and catalyst V were added to toluene. Next, unsaturated aldehyde 1a was added and th