181115-89-9

Basic information

• Product Name: Benzoic acid (2R,3R,4S,5R,6R)-6-[(2R,3R,4S,5R,6R)-6-allyloxy-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yloxy]-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yl ester
• Synonyms: Benzoic acid (2R,3R,4S,5R,6R)-6-[(2R,3R,4S,5R,6R)-6-allyloxy-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yloxy]-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yl ester
• CAS NO: 181115-89-9
• Molecular Weight: 1207.38
• Mol File: 181115-89-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid (2R,3R,4S,5R,6R)-6-[(2R,3R,4S,5R,6R)-6-allyloxy-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yloxy]-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid (2R,3R,4S,5R,6R)-6-[(2R,3R,4S,5R,6R)-6-allyloxy-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yloxy]-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yl ester(181115-89-9)
• EPA Substance Registry System: Benzoic acid (2R,3R,4S,5R,6R)-6-[(2R,3R,4S,5R,6R)-6-allyloxy-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yloxy]-4,5-bis-(4-methoxy-benzyloxy)-2-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3-yl ester(181115-89-9)

Safety Data

• Hazardous Substances Data: 181115-89-9(Hazardous Substances Data)

Upstream product

• 3616-19-1 1,2,3,6,2',3',4',6'-octa-O-acetylmaltose 
• 4753-07-5 α-hepta-O-acetylmaltosyl bromide 
• 98-88-4 benzoyl chloride 
• 181115-83-3 allyl 2,3,6-tri-O-4-methoxybenzyl-4-O-(2,3,6-tri-O-4-methoxybenzyl-α-D-glucopyranosyl)-β-D-glucopyranoside 
• 113842-87-8 allyl α-D-glucopyranosyl-(1->4)-β-D-glcopyranoside 
• 97777-13-4 allyl O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-acetyl-β-D-gluco-pyranoside 

Relevant articles and documents

Two interconverting glycophanes from maltose

Two new glycophanes, 1 and 3, that interconvert through transesterification in water at room temperature are presented. The synthesis, properties of interconvertion and preliminary binding and conformational studies of these macrocycles are also described.