1352964-75-0

Basic information

• Product Name: benzyl (2S,9R,E)-1-(tert-butyldimethylsilyloxy)-9-hydroxy-6-oxotridec-4-en-2-ylcarbamate
• Synonyms: benzyl (2S,9R,E)-1-(tert-butyldimethylsilyloxy)-9-hydroxy-6-oxotridec-4-en-2-ylcarbamate
• CAS NO: 1352964-75-0
• Molecular Weight: 491.744
• Mol File: 1352964-75-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl (2S,9R,E)-1-(tert-butyldimethylsilyloxy)-9-hydroxy-6-oxotridec-4-en-2-ylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (2S,9R,E)-1-(tert-butyldimethylsilyloxy)-9-hydroxy-6-oxotridec-4-en-2-ylcarbamate(1352964-75-0)
• EPA Substance Registry System: benzyl (2S,9R,E)-1-(tert-butyldimethylsilyloxy)-9-hydroxy-6-oxotridec-4-en-2-ylcarbamate(1352964-75-0)

Safety Data

• Hazardous Substances Data: 1352964-75-0(Hazardous Substances Data)

Upstream product

• 107736-67-4 (R)-ethyl 4-hydroxyoctanoate 
• 142545-26-4 3(S)-Benzyloxycarbonylamino-4-tert-butyldimethylsilyloxypropanecarboxylic acid methyl ester 
• 66-25-1 hexanal 
• 1352964-64-7 (S)-benzyl 1-(tert-butyldimethylsilyloxy)-4-oxobutan-2-ylcarbamate 
• 1352964-82-9 (R)-dimethyl 5-hydroxy-2-oxononylphosphonate 

Relevant articles and documents

Enantioselective access to (-)-indolizidines 167B, 209D, 239AB, 195B and (-)-monomorine from a common chiral synthon

An enantioselective access to (-)-indolizidine alkaloids 167B, 209D, 239AB, 195B and (-)-monomorine from a new chiral synthon is described. The use of (S)-3-(Cbz-amino)-4-(tert-butyldimethylsilyloxy)butanal, obtained from l-aspartic acid, has provided eff