99393-14-3

Basic information

• Product Name: R-(+) estere benzilico dell'acido γ-butirrolatton-γ-3-propionico
• Synonyms: R-(+) estere benzilico dell'acido γ-butirrolatton-γ-3-propionico
• CAS NO: 99393-14-3
• Molecular Weight: 248.279
• Mol File: 99393-14-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: R-(+) estere benzilico dell'acido γ-butirrolatton-γ-3-propionico(CAS DataBase Reference)
• NIST Chemistry Reference: R-(+) estere benzilico dell'acido γ-butirrolatton-γ-3-propionico(99393-14-3)
• EPA Substance Registry System: R-(+) estere benzilico dell'acido γ-butirrolatton-γ-3-propionico(99393-14-3)

Safety Data

• Hazardous Substances Data: 99393-14-3(Hazardous Substances Data)

Upstream product

• 122950-95-2 Dibenzyl γ-hydroxypimelate 
• 502-50-1 4-Ketopimelic acid 
• 70957-27-6 Dibenzyl γ-oxopimelate 
• 100-39-0 benzyl bromide 
• 42998-51-6 benzyl ethyl malonate 
• 58879-33-7 (R)-(-)-γ-<(tosyloxy)methyl>-γ-butyrolactone 
• 99393-06-3 R-(-)-γ-bromomethylene-γ-butyrolactone 

Downstream Products

• 98611-83-7 (S)-3-(5-oxotetrahydro-2-furanyl)propanoic acid 
• 93787-95-2 (R)-((E)-5-Hex-3-enyl)-dihydro-furan-2-one 
• 155682-86-3 (R)-(+)-γ-jasmolactone 
• 98611-86-0 S-(-)-γ-butyrolactone-γ-3-propionic acid 

Relevant articles and documents

Enantioselective synthesis of (-)-γ-jasmolactone

The title compound was prepared in seven steps starting from the commercially available 4-ketopimelic acid. The key step features an enantioselective lactonization promoted by PPL.

Synthesis of the S-(-) and R-(+)-enantiomers of γ-butyrrolacton-γ-3-propionic acid

-