121614-12-8

Basic information

• Product Name: tert-butyl (4S)-3--4,5-(isopropylidenedioxy)pentanoate
• CAS NO: 121614-12-8
• Molecular Weight: 479.733
• Mol File: 121614-12-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl (4S)-3--4,5-(isopropylidenedioxy)pentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (4S)-3--4,5-(isopropylidenedioxy)pentanoate(121614-12-8)
• EPA Substance Registry System: tert-butyl (4S)-3--4,5-(isopropylidenedioxy)pentanoate(121614-12-8)

Safety Data

• Hazardous Substances Data: 121614-12-8(Hazardous Substances Data)

Upstream product

• 53933-47-4 N-((1S)-1-phenylethyl)hydroxylamine 
• 15186-48-8 2,3-isopropylidene-glyceraldehyde 
• 74786-02-0 1-(tert-butyldimethylsilyloxy)-1-tert-butoxyethylene 
• 121614-03-7 (1R)-N-<<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>methylene>-1-phenylethylamine N-oxide 
• 2912-98-3 (R)-1-Phenylethylhydroxylamine 

Downstream Products

• 121701-19-7 (3R,4S)-5-acetoxy-3-benzoylamino-4-pentanolide 
• 121701-20-0 (3S,4S)-5-acetoxy-3-benzoylamino-4-pentanolide 
• 126569-20-8 3-benzoylamino-2,3-dideoxy-D-ribo-pentapyranose 
• 126569-22-0 tert-butyl (4S)-3-benzoylamino-4,5-(isopropylidenedioxy)pentanoate 

Relevant articles and documents

Chemistry of O-Silylated Ketene Acetals: Stereocontrolled Synthesis of 3-Benzoylamino-2,3-dideoxypentoses by a 1,3-Addition to Chiral Nitrones

The stereochemistry of 1,3-addition of ketene acetals (1a,b) to the chiral nitrones (4a-d) derived from 2,3-O-isopropylidene-D-glyceraldehyde was examined.The reaction of ketene methyl tert-butyldimethylsilyl acetal (1a) with the N-benzylnitrone (4a) prod