99388-74-6

Basic information

• Product Name: Benzyl 4-O-(2,4-di-O-benzyl-α-D-xylopyranosyl)-2,3-di-O-benzyl-α-D-xylopyranoside
• Synonyms: Benzyl 4-O-(2,4-di-O-benzyl-α-D-xylopyranosyl)-2,3-di-O-benzyl-α-D-xylopyranoside
• CAS NO: 99388-74-6
• Molecular Weight: 732.871
• Mol File: 99388-74-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzyl 4-O-(2,4-di-O-benzyl-α-D-xylopyranosyl)-2,3-di-O-benzyl-α-D-xylopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 4-O-(2,4-di-O-benzyl-α-D-xylopyranosyl)-2,3-di-O-benzyl-α-D-xylopyranoside(99388-74-6)
• EPA Substance Registry System: Benzyl 4-O-(2,4-di-O-benzyl-α-D-xylopyranosyl)-2,3-di-O-benzyl-α-D-xylopyranoside(99388-74-6)

Safety Data

• Hazardous Substances Data: 99388-74-6(Hazardous Substances Data)

Upstream product

• 99388-71-3 Benzyl 4-O-(3-O-Allyl-2,4-di-O-benzyl-α-D-xylopyranosyl)-2,3-di-O-benzyl-α-D-xylopyranoside 
• 889874-12-8 Benzyl 2,3-di-O-benzyl-α-D-xylopyranoside 
• 99388-80-4 Acetic acid (2R,3R,4S,5R)-3,5-bis-benzyloxy-2-(2-methoxy-ethoxy)-tetrahydro-pyran-4-yl ester 
• 18403-12-8 benzyl β-D-xylopyranoside 
• 100-51-6 benzyl alcohol 
• 99388-81-5 Benzoic acid (2R,3R,4S,5R)-3,5-bis-benzyloxy-2-(2-methoxy-ethoxy)-tetrahydro-pyran-4-yl ester 
• 99388-83-7 (2S,3R,4S,5R)-5-Allyloxy-2,3,4-tris-benzyloxy-tetrahydro-pyran 
• 99388-63-3 2-Methoxyethyl 2,4-di-O-benzyl-β-D-xylopyranoside 
• 127874-66-2 3-O-acetyl-2,4-di-O-benzyl-α,β-D-xylopyranose 
• 99388-85-9 (2S,3R,4S,5R)-4-Allyloxy-3,5-bis-benzyloxy-2-methoxy-tetrahydro-pyran 
• 127874-68-4 3-O-Allyl-2,4-di-O-benzyl-D-xylopyranose 
• 99388-82-6 C₂₁H₂₈O₅ 
• 99388-64-4 Benzyl 2,3-O-cyclohexylidene-α-D-xylopyranoside 
• 99388-84-8 (2S,3R,4R,5R)-5-Allyloxy-2-benzyloxy-tetrahydro-pyran-3,4-diol 

Relevant articles and documents

Pentoside Synthesis by Dehydrative Glykosylation. Synthesis of O-α-L-Arabinofuranosyl-(1-3)-O-β-D-xylopyranosyl-(1-4)-D-xylopyranose

O-α-L-Arabinofuranosyl-(1-3)-O-β-D-xylopyranosyl-(1-4)-D-xylopyranose isolated from the hydrolyzate of corncobs arabinoxylan was synthesized by way of dehydrative glycosylation.