1291065-78-5

Basic information

• Product Name: tert-butyl {2,3-dimethyl-1-(phenylsulfonyl)but-2-en-1-yl}carbamate
• Synonyms: tert-butyl {2,3-dimethyl-1-(phenylsulfonyl)but-2-en-1-yl}carbamate
• CAS NO: 1291065-78-5
• Molecular Weight: 325.429
• Mol File: 1291065-78-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl {2,3-dimethyl-1-(phenylsulfonyl)but-2-en-1-yl}carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl {2,3-dimethyl-1-(phenylsulfonyl)but-2-en-1-yl}carbamate(1291065-78-5)
• EPA Substance Registry System: tert-butyl {2,3-dimethyl-1-(phenylsulfonyl)but-2-en-1-yl}carbamate(1291065-78-5)

Safety Data

• Hazardous Substances Data: 1291065-78-5(Hazardous Substances Data)

Upstream product

• 107-86-8 3,3-dimethyl acrylaldehyde 
• 4248-19-5 tert-butyl carbazate 
• 618-41-7 Benzenesulfinic acid 
• 873-55-2 sodium benzenesulfonate 

Downstream Products

• 69805-63-6 methyl 2-((tert-butoxycarbonyl)amino)-4-methylpentanoate 
• 69942-12-7 N-tert-butoxycarbonylserine methyl ester 
• 31954-27-5 N-(tert-butoxycarbonyl)glycine methyl ester 
• 1415303-95-5 C₁₈H₂₉NO₂Si 

Relevant articles and documents

Catalytic Asymmetric Diels-Alder Reaction of Quinone Imine Ketals: A Site-Divergent Approach

The catalytic asymmetric Diels-Alder reaction of quinone imine ketals with diene carbamates catalyzed by axially chiral dicarboxylic acids is reported herein. A variety of primary and secondary alkyl-substituted quinone derivatives which have not been applied in previous asymmetric quinone Diels-Alder reactions could be employed using this method. More importantly, we succeeded in developing a strategy to divert the reaction site in unsymmetrical 3-alkyl quinone imine ketals from the inherently favored unsubstituted C=C bond to the disfavored alkyl-substituted C=C bond.