937181-61-8

Basic information

• Product Name: 1-[5-O-(tert-butyldimethylsilyl)-3-deoxy-3,4-C-(difluoromethylene)-2-O-(4-methoxybenzyl)-α-L-arabinofuranosyl]-3-(4-methoxybenzyl)uracil
• Synonyms: 1-[5-O-(tert-butyldimethylsilyl)-3-deoxy-3,4-C-(difluoromethylene)-2-O-(4-methoxybenzyl)-α-L-arabinofuranosyl]-3-(4-methoxybenzyl)uracil
• CAS NO: 937181-61-8
• Molecular Weight: 630.761
• Mol File: 937181-61-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-[5-O-(tert-butyldimethylsilyl)-3-deoxy-3,4-C-(difluoromethylene)-2-O-(4-methoxybenzyl)-α-L-arabinofuranosyl]-3-(4-methoxybenzyl)uracil(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[5-O-(tert-butyldimethylsilyl)-3-deoxy-3,4-C-(difluoromethylene)-2-O-(4-methoxybenzyl)-α-L-arabinofuranosyl]-3-(4-methoxybenzyl)uracil(937181-61-8)
• EPA Substance Registry System: 1-[5-O-(tert-butyldimethylsilyl)-3-deoxy-3,4-C-(difluoromethylene)-2-O-(4-methoxybenzyl)-α-L-arabinofuranosyl]-3-(4-methoxybenzyl)uracil(937181-61-8)

Safety Data

• Hazardous Substances Data: 937181-61-8(Hazardous Substances Data)

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 937181-54-9 1-[5-O-(tert-butyldimethylsilyl)-3-deoxy-3-iodo-2-O-(4-methoxybenzyl)-β-D-xylofuranosyl]-3-(4-methoxybenzyl)uracil 
• 937181-53-8 5'-O-(tert-butyldimethylsilyl)-3-N,2'-O-di(4-methoxybenzyl)uridine 
• 937181-55-0 1-[5-O-(tert-butyldimethylsilyl)-3-deoxy-2-O-(4-methoxybenzyl)-β-D-glycero-pent-3-enofuranosyl]-3-(4-methoxybenzyl)uracil 
• 371-76-6 bis(trifluoromethyl)mercury 

Downstream Products

• 937181-62-9 C₁₈H₁₈F₂N₂O₆ 
• 937181-63-0 1-[2,5-di-O-acetyl-3-deoxy-3,4-C-(difluoromethylene)-α-L-arabinofuranosyl]-3-(4-methoxybenzyl)uracil 

Relevant articles and documents

Synthesis of 3′-deoxynucleosides with 2-oxabicyclo[3.1.0]hexane sugar moieties: Addition of difluorocarbene to a 3′,4′-unsaturated uridine derivative and 1,2-dihydrofurans derived from D- and L-xylose

(Chemical Equation Presented) Syntheses of 3′-deoxy analogues of adenosine, cytidine, and uridine with a 2,2-difluorocyclopropane ring fused at C3′-C4′ are described. Treatment of a 2′,5′-protected- 3′,4′-unsaturated derivative of uridine with difluorocar