215436-53-6

Basic information

• Product Name: cis-2-benzoyloxymethyl-4-(N₄'-acetylcytosin-1'-yl)-1,3-oxathiolane
• CAS NO: 215436-53-6
• Molecular Weight: 375.405
• Mol File: 215436-53-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: cis-2-benzoyloxymethyl-4-(N₄'-acetylcytosin-1'-yl)-1,3-oxathiolane(CAS DataBase Reference)
• NIST Chemistry Reference: cis-2-benzoyloxymethyl-4-(N₄'-acetylcytosin-1'-yl)-1,3-oxathiolane(215436-53-6)
• EPA Substance Registry System: cis-2-benzoyloxymethyl-4-(N₄'-acetylcytosin-1'-yl)-1,3-oxathiolane(215436-53-6)

Safety Data

• Hazardous Substances Data: 215436-53-6(Hazardous Substances Data)

Upstream product

• 14631-20-0 4-N-Acetylcytosine 
• 143338-44-7 2-[(phenylcarbonyloxy)methyl]-1,3-oxathiolane 

Downstream Products

• 160707-69-7 trans-2-hydroxymethyl-4-(cytosin-1'-yl)-1,3-oxathiolane 

Relevant articles and documents

A new strategy for the asymmetric synthesis of 1,3-oxathiolane-based nucleoside analogues

A ready asymmetric synthesis of 3'-oxathionucleosides has been accomplished in three main steps from benzoyloxyethanal. The synthesis is characterized by high overall yield and considerable enantiomeric excesses. It represents a general synthetic path to prepare a wide range of heterosubstituted sulfur-containing nucleoside analogues.