Basic information Safety Supplier Related

BENZYL 2-O-BENZYL-4,6-O-BENZYLIDENE-ALPHA-D-MANNOPYRANOSIDE

Basic information Safety Supplier Related

BENZYL 2-O-BENZYL-4,6-O-BENZYLIDENE-ALPHA-D-MANNOPYRANOSIDE Basic information

Product Name:
BENZYL 2-O-BENZYL-4,6-O-BENZYLIDENE-ALPHA-D-MANNOPYRANOSIDE
Synonyms:
  • 1,2-Di-O-benzyl-4,6-O-benzylidene-a-D-mannopyranoside
  • Benzyl 2-O-Benzyl-4,6-O-benzylidene-α-D-mannopyranoside
  • PhenylMethyl 2-O-(PhenylMethyl)-4,6-O-(phenylMethylene)-α-D-Mannopyranoside
  • α-D-Mannopyranoside, phenylmethyl 2-O-(phenylmethyl)-4,6-O-(phenylmethylene)-
  • Benzyl-2-O-benzyl-4,6-O-benzyliden-α-D-mannopyranosid
  • Benzyl 2-O-Benzyl-4,6-O-benzylidene-α-D-mannopyranoside, CAS 40983-95-7
CAS:
40983-95-7
MF:
C27H28O6
MW:
448.51
Product Categories:
  • 13C & 2H Sugars
  • Carbohydrates & Derivatives
Mol File:
40983-95-7.mol
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BENZYL 2-O-BENZYL-4,6-O-BENZYLIDENE-ALPHA-D-MANNOPYRANOSIDE Chemical Properties

Boiling point:
619.4±55.0 °C(Predicted)
Density 
1.28±0.1 g/cm3(Predicted)
pka
12.68±0.70(Predicted)
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BENZYL 2-O-BENZYL-4,6-O-BENZYLIDENE-ALPHA-D-MANNOPYRANOSIDE Usage And Synthesis

Uses

Benzyl 2-O-Benzyl-4,6-O-benzylidene-α-D-mannopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].

References

[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922

BENZYL 2-O-BENZYL-4,6-O-BENZYLIDENE-ALPHA-D-MANNOPYRANOSIDESupplier

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