Basic information Safety Supplier Related

Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside

Basic information Safety Supplier Related

Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside Basic information

Product Name:
Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside
Synonyms:
  • Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside
  • Phenylmethyl 3-O-(Phenylmethyl)-4,6-O-(phenylmethylene))-a-D-mannopyranoside
  • Benzyl 3-O-Benzyl-4,6-O-benzylidene-α-D-mannopyranoside
  • Phenylmethyl 3-O-(Phenylmethyl)-4,6-O-(phenylmethylene))-α-D-mannopyranoside
  • 1,3-Di-O-benzyl-4,6-O-benzylidene-a-D-mannopyranoside
  • α-D-Mannopyranoside, phenylmethyl 3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-
  • Benzyl 3-O-Benzyl-4,6-O-benzylidene-α-D-mannopyranoside
CAS:
62774-16-7
MF:
C27H28O6
MW:
448.51
Product Categories:
  • Carbohydrates & Derivatives
  • 13C & 2H Sugars
Mol File:
62774-16-7.mol
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Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside Chemical Properties

solubility 
Chloroform, Dichloromethane
form 
Oil
color 
Colorless
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Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside Usage And Synthesis

Chemical Properties

Colorless Oil

Uses

Phenylmethyl 3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-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

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