219906-49-7

Basic information

• Product Name: benzyl 2-O-(4-methoxybenzoyl)-α-D-xylopyranoside
• Synonyms: benzyl 2-O-(4-methoxybenzoyl)-α-D-xylopyranoside
• CAS NO: 219906-49-7
• Molecular Weight: 374.39
• Mol File: 219906-49-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: benzyl 2-O-(4-methoxybenzoyl)-α-D-xylopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2-O-(4-methoxybenzoyl)-α-D-xylopyranoside(219906-49-7)
• EPA Substance Registry System: benzyl 2-O-(4-methoxybenzoyl)-α-D-xylopyranoside(219906-49-7)

Safety Data

• Hazardous Substances Data: 219906-49-7(Hazardous Substances Data)

Upstream product

• 100-07-2 4-methoxy-benzoyl chloride 
• 18403-12-8 benzyl β-D-xylopyranoside 
• 100-51-6 benzyl alcohol 
• 6763-34-4 D-xylose 

Downstream Products

• 219906-50-0 4-Methoxy-benzoic acid (2S,3R,4R,5R)-2-benzyloxy-4,5-bis-triethylsilanyloxy-tetrahydro-pyran-3-yl ester 
• 219906-58-8 C₇₃H₁₂₈O₁₆Si₄ 
• 321125-08-0 2-O-(4-methoxybenzoyl)-3,4-di-O-triethylsilyl-β-D-xylopyranosyl-(1→3)-2-O-acetyl-4-O-triethylsilyl-α,β-L-arabinopyranosyl trichloroacetimidate 
• 219906-55-5 4-Methoxy-benzoic acid (2S,3R,4R,5R)-2-((2S,3R,4R,5S)-3-acetoxy-2-benzyloxy-5-triethylsilanyloxy-tetrahydro-pyran-4-yloxy)-4,5-bis-triethylsilanyloxy-tetrahydro-pyran-3-yl ester 
• 219906-53-3 4-Methoxy-benzoic acid (2S,3R,4R,5R)-2-((2S,3R,4S,5S)-3-acetoxy-2-benzyloxy-5-hydroxy-tetrahydro-pyran-4-yloxy)-4,5-bis-triethylsilanyloxy-tetrahydro-pyran-3-yl ester 
• 219906-54-4 4-Methoxy-benzoic acid (2S,3R,4R,5R)-2-((3S,4S,5R,6S)-5-acetoxy-6-benzyloxy-4-hydroxy-tetrahydro-pyran-3-yloxy)-4,5-bis-triethylsilanyloxy-tetrahydro-pyran-3-yl ester 
• 321125-07-9 2-O-(4-methoxybenzoyl)-3,4-di-O-triethylsilyl-α,β-D-xylopyranosyl trichloroacetimidate 
• 145075-81-6 3β,16β,17α-trihydroxycholest-5-en-22-one 16-O-{O-[2-O-(4-methoxybenzoyl)-β-D-xylopyranosyl]-(1->3)-2-O-acetyl-β-L-arabinopyranoside} 

Relevant articles and documents

Synthesis, conformational analysis and SAR research of OSW-1 analogues

A series of novel OSW-1 analogues were synthesized by coupling disaccharides (2-O-4-methoxylbenzoyl-β-D-xylopyranosyl-(1→3)-2-O-acetyl-α-L-arabinopyranosyl) or (2-O-4-(E)-cinnamoyl-β-D-xylopyranosyl-(1→3)-2-O-acetyl-α-L-arabinopyranosyl) and their 1→4 lin