CAS 641635-63-4

Formula: C28H32O6

InChI: InChI=1S/C28H32O6/c1-30-28-27(33-20-23-15-9-4-10-16-23)26(32-19-22-13-7-3-8-14-22)25(24(17-29)34-28)31-18-21-11-5-2-6-12-21/h2-16,24-29H,17-20H2,1H3/t24-,25+,26+,27-,28?/m1/s1

InChI key: MOKYEUQDXDKNDX-PBVUBXADSA-N

SMILES: COC1[C@@H]([C@H]([C@H]([C@H](O1)CO)OCC2=CC=CC=C2)OCC3=CC=CC=C3)OCC4=CC=CC=C4

Methyl 2,3,4-Tri-O-benzyl-D-galactopyranoside

CAS: 641635-63-4

Methyl 2,3,4-Tri-O-benzyl-D-galactopyranoside is a biochemical reagent used in the study of glycobiology. Glycobiology examines the structure, synthesis, biology, and evolution of sugars, including aspects such as carbohydrate chemistry, glycan synthesis and degradation enzymology, protein-glycan interactions, and the role of glycans in biological systems. This field is closely linked to fundamental research, biomedicine, and biotechnology.

Formula: C₂₈H₃₂O₆

Color and Shape: Solid

Molecular weight: 464.55

Ref: TM-TSW-00609

Methyl 2,3,4-Tri-O-benzyl-D-galactopyranoside

Controlled Product

CAS: 641635-63-4

Formula: C₂₈H₃₂O₆

Color and Shape: Neat

Molecular weight: 464.55

Ref: TR-M330813

Methyl 2,3,4-tri-O-benzyl-D-galactopyranoside

CAS: 641635-63-4

Methyl 2,3,4-tri-O-benzyl-D-galactopyranoside is an Oligosaccharide that contains three benzyl groups. It is a custom synthesis and can be modified to create complex carbohydrates. Methyl 2,3,4-tri-O-benzyl-D-galactopyranoside has been synthesized by the click modification of galactose with triacetoxybenzene. This compound has been shown to have antiinflammatory activity in vitro.

Formula: C₂₈H₃₂O₆

Purity: Min. 95%

Molecular weight: 464.56 g/mol

Ref: 3D-MM07262