14645-36-4

Basic information

• Product Name: methyl 5-O-triphenylmethyl-α-L-arabonofuranoside
• Synonyms: methyl 5-O-triphenylmethyl-α-L-arabonofuranoside
• CAS NO: 14645-36-4
• Molecular Weight: 406.478
• Mol File: 14645-36-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 5-O-triphenylmethyl-α-L-arabonofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5-O-triphenylmethyl-α-L-arabonofuranoside(14645-36-4)
• EPA Substance Registry System: methyl 5-O-triphenylmethyl-α-L-arabonofuranoside(14645-36-4)

Safety Data

• Hazardous Substances Data: 14645-36-4(Hazardous Substances Data)

Upstream product

• 532-20-7 L-arabinose 
• 42793-97-5 2,3,5-tri-O-benzoyl-1-O-methyl-α-L-arabinofuranose 
• 76-83-5 trityl chloride 
• 3795-68-4 methyl α-L-arabinofuranoside 

Downstream Products

• 16896-01-8 methyl 2,3-di-O-benzyl-5-O-triphenylmethyl-α-L-arabinofuranoside 
• 1422008-00-1 methyl 6,6-dibromo-2,3-di-O-benzyl-5,6-dideoxy-β-L-arabino-hex-5-enofuranoside 
• 16896-05-2 methyl 6,6-dibromo-2,3-di-O-benzyl-5,6-dideoxy-β-L-arabino-hex-5-enofuranoside 
• 1422008-01-2 methyl 2,3-di-O-benzyl-5,6-dideoxy-β-L-arabino-hex-5-yofuranoside 
• 1422007-98-4 methyl 5,6-tetradehydro-5,6,7,10-tetradeoxy-7,10-hydroxylamino-2,3,8,9,11,12-hexa-O-benzyl-D-galacto-β-D-galacto-dodecafuranose 
• 17229-98-0 methyl 5-O-trityl-2,3-anhydro-α-L-lyxofuranoside 
• 527682-23-1 methyl 5-O-(2,3-anhydro-β-L-lyxofuranosyl)-2,3-di-O-benzyl-α-L-arabinofuranoside 
• 527682-21-9 methyl 5-O-(2,3-anhydro-β-D-lyxofuranosyl)-2,3-di-O-benzyl-α-L-arabinofuranoside 
• 16896-03-0 methyl 2,3-di-O-benzyl-α-L-arabinofuranoside 
• 283173-88-6 methyl 2,3-di-O-pivaloyl-5-O-triphenylmethyl-α-L-arabonofuranoside 
• 76690-31-8 methyl 2,3-di-O-acetyl-5-O-trityl-α-L-arabinofuranoside 

Relevant articles and documents

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2,3-Anhydro sugars in glycoside bond synthesis. Highly stereoselective syntheses of oligosaccharides containing α- and β-arabinofuranosyl linkages

The ever-increasing discovery of biologically important events mediated by carbohydrates has generated great interest in the synthesis of oligosaccharides and the development of new methods for glycosidic bond formation. In this paper, we report that 2,3-