404344-93-0

Basic information

• Product Name: (2S,3R,4R)-4-benzyloxymethyl-2,3-isopropylidenedioxy-1-methylenecyclopentane
• Synonyms: (2S,3R,4R)-4-benzyloxymethyl-2,3-isopropylidenedioxy-1-methylenecyclopentane
• CAS NO: 404344-93-0
• Molecular Weight: 274.36
• Mol File: 404344-93-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3R,4R)-4-benzyloxymethyl-2,3-isopropylidenedioxy-1-methylenecyclopentane(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4R)-4-benzyloxymethyl-2,3-isopropylidenedioxy-1-methylenecyclopentane(404344-93-0)
• EPA Substance Registry System: (2S,3R,4R)-4-benzyloxymethyl-2,3-isopropylidenedioxy-1-methylenecyclopentane(404344-93-0)

Safety Data

• Hazardous Substances Data: 404344-93-0(Hazardous Substances Data)

Upstream product

• 404345-13-7 (1R,2S,3R,4R)-4-acetoxymethyl-1-iodomethyl-2,3-isopropylidenedioxycyclopentane 
• 404344-91-8 (2S,3R,4R)-4-acetoxymethyl-2,3-isopropylidenedioxy-1-methylenecyclopentane 
• 145260-33-9 (1R,2R,3S,4S)-(4-hydroxymethyl-2,3-isopropylidenedioxy-1-cyclopentyl)methyl acetate 
• 59210-93-4 (2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4,6-diyl)dimethanol 
• 100-51-6 benzyl alcohol 
• 404344-92-9 (2S,3R,4R)-4-methanol-2,3-isopropylidenedioxy-1-methylenecyclopentane 

Downstream Products

• 5817-70-9 methyl N-benzylcarbamate 

Relevant articles and documents

Enantioselective route to key intermediates in the synthesis of carbocyclic phosphoribosyltransferase transition state analogues

The enantioselective preparation of key intermediates in the synthesis of transition state analogues of hypoxanthine-guanine phosphoribosyltransferase, (1S,2S,3R,4R)-4-acetoxymethyl-1-bromomethyl-2,3-isopropylidenedioxy-1- toluenesulfonamidocyclopentane (3a) and the 4-nitrobenzenesulfonamido analogue (3b), are described.