137119-40-5

Basic information

• Product Name: methyl 4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside
• Synonyms: methyl 4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside
• CAS NO: 137119-40-5
• Molecular Weight: 444.436
• Mol File: 137119-40-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside(137119-40-5)
• EPA Substance Registry System: methyl 4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside(137119-40-5)

Safety Data

• Hazardous Substances Data: 137119-40-5(Hazardous Substances Data)

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 7216-69-5 methyl β-D-lactopyranoside 

Downstream Products

• 57472-05-6 methyl 2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 136963-00-3 methyl 2,3-di-O-acetyl-6-bromo-6-deoxy-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 69988-36-9 methyl 4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-6-bromo-6-deoxy-β-D-glucopyranoside 2,3,2',3'-tetraacetate 
• 312700-90-6 C₈₁H₈₂O₁₅Si 
• 312701-15-8 C₇₂H₇₄N₂O₁₅SSi 
• 312700-87-1 C₆₈H₇₂O₁₅Si 
• 312701-13-6 C₆₈H₇₀O₁₅Si 
• 312700-88-2 C₆₈H₇₂O₁₄Si 
• 312701-17-0 C₆₅H₆₄O₁₅ 
• 312701-16-9 C₆₁H₆₆O₁₄Si 
• 345320-70-9 Methyl 2,3-di-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-6-O-(tert-butyldimethylsilyl)-β-D-glucopyranoside 
• 345320-77-6 Methyl 2,3-di-O-benzyl-4-O-(2,3-di-O-benzyl-6-O-benzoyl-β-D-galactopyranosyl)-6-O-methoxycarbonylmethyl-β-D-glucopyranoside 
• 345320-75-4 Methyl 2,3-di-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-6-O-methoxycarbonylmethyl-β-D-glucopyranoside 
• 108282-43-5 methyl 2-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranosyl-(1->4)-O-2,3,6-tri-O-benzoyl-β-D-glucopyranoside 

Relevant articles and documents

Chemical synthesis using enzymatically generated building units for construction of the human milk pentasaccharides sialyllacto-N-tetraose and sialyllacto-N-neotetraose epimer

α,2-3- and α,2-6-sialylated lactosaminide precursor structures obtained by various enzymatic procedures could be used for glycosylations employing triflic acid/N-iodosuccinimide. Easily accessible selectively protected lactoside derivatives served as acce