188559-09-3

Basic information

• Product Name: (2R,3R)-5,5-Bis-benzyloxy-1-trityloxy-pentane-2,3-diol
• CAS NO: 188559-09-3
• Molecular Weight: 574.717
• Mol File: 188559-09-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R)-5,5-Bis-benzyloxy-1-trityloxy-pentane-2,3-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-5,5-Bis-benzyloxy-1-trityloxy-pentane-2,3-diol(188559-09-3)
• EPA Substance Registry System: (2R,3R)-5,5-Bis-benzyloxy-1-trityloxy-pentane-2,3-diol(188559-09-3)

Safety Data

• Hazardous Substances Data: 188559-09-3(Hazardous Substances Data)

Upstream product

• 100-51-6 benzyl alcohol 
• 134485-39-5 (E)-5,5-Bis-benzyloxy-pent-2-enoic acid ethyl ester 
• 134485-30-6 ethyl-3,3-di(benzyl)oxypropanoate 
• 134485-38-4 3,3-dibenzyloxypropanal 
• 134485-31-7 5,5-Dibenzyloxy-2E-penten-1-ol 
• 188559-06-0 C₃₈H₃₆O₃ 

Downstream Products

• 84472-83-3 1-[2-deoxy-5-O-(triphenylmethyl)-β-D-xylofuranosyl]uracil 
• 13039-99-1 1-[2-deoxy-β-D-threo-pentofuranosyl]uracil 
• 188559-32-2 4-Allyloxy-2-((2R,3R)-5-benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-5-chloro-pyrimidine 
• 188559-30-0 4-Allyloxy-2-((2R,3R)-5-benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-5-methyl-pyrimidine 
• 188559-31-1 4-Allyloxy-2-((2R,3R)-5-benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-pyrimidine 
• 188559-37-7 2-((2R,3R)-5-Benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-5-chloro-3H-pyrimidin-4-one 
• 188559-35-5 2-((2R,3R)-5-Benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-5-methyl-3H-pyrimidin-4-one 
• 188559-36-6 2-((2R,3R)-5-Benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-3H-pyrimidin-4-one 
• 188559-40-2 5-Chloro-1-((2R,4R,5R)-4-hydroxy-5-trityloxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione 
• 188559-43-5 5'-O-trityl-O²,3'-cycloanhydro-N³-thymidine 
• 188559-94-6 1-(2-deoxy-β-D-lyxofuranosyl)-5-chlorouracil 

Relevant articles and documents

Stereocontrolled synthesis of β-2'-deoxypyrimidine nucleosides via intramolecular glycosylations

A pyrimidine moiety was tethered at the 3'-β-position of D-threo-furanosides. By carefully controlling the reaction conditions, pyrimidine bases can be delivered to the anomeric center to give of β-pyrimidine nucleosides in good yield and with complete stereocontrol.