1393922-94-5

Basic information

• Product Name: (2R,3S,5S)-5-thymino-2-(tert-butyldimethyl)silyloxymethyl-3-benzyloxycyclopentanone
• CAS NO: 1393922-94-5
• Molecular Weight: 458.63
• Mol File: 1393922-94-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S,5S)-5-thymino-2-(tert-butyldimethyl)silyloxymethyl-3-benzyloxycyclopentanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S,5S)-5-thymino-2-(tert-butyldimethyl)silyloxymethyl-3-benzyloxycyclopentanone(1393922-94-5)
• EPA Substance Registry System: (2R,3S,5S)-5-thymino-2-(tert-butyldimethyl)silyloxymethyl-3-benzyloxycyclopentanone(1393922-94-5)

Safety Data

• Hazardous Substances Data: 1393922-94-5(Hazardous Substances Data)

Upstream product

• 1393922-90-1 (2R,3S)-2-(tert-butyldimethylsilyl)oxymethyl-3-benzyloxy-6-oxabicylo[3.1.0]hexane 
• 117641-39-1 (2R,3S)-2-benzyloxymethyl-6-oxabicyclo<3.1.0>hexan-3-ol 
• 117641-42-6 (1S,2R,3S,5R)-2-Hydroxymethyl-6-oxa-bicyclo[3.1.0]hexan-3-ol 

Relevant articles and documents

Essential reactive intermediates in nucleoside chemistry: Cyclonucleoside cations

DFT-based modeling as well as experimental examination of model keto nucleosides have revealed that high susceptibility of these compounds to acids is due to formation of intermediate cyclonucleoside cations of low energy. Theoretically established chemical structures of these previously overlooked intermediates explain the reaction courses for a cluster of nucleoside reactions.