| Identification | Back Directory | [Name]
BENZYL 2,3,4-TRI-O-BENZYL-ALPHA-D-MANNOPYRANOSIDE | [CAS]
57783-76-3 | [Synonyms]
1,2,3,4-Tetra-O-benzyl-a-D-mannopyranoside
Benzyl 2,3,4-Tri-O-benzyl-α-D-mannopyranoside
Benzyl 2,3,4-tri-O-benzyl-alpha-D-mannopyranoside, Min. 98%
PhenylMethyl 2,3,4-Tris-O-(phenylMethyl)-α-D-Mannopyranoside
α-D-Mannopyranoside, phenylmethyl 2,3,4-tris-O-(phenylmethyl)-
((2R,3R,4S,5S,6S)-3,4,5,6-tetrakis(benzyloxy)tetrahydro-2H-pyran-2-yl)methanol | [Molecular Formula]
C34H36O6 | [MDL Number]
MFCD03425507 | [MOL File]
57783-76-3.mol | [Molecular Weight]
540.65 |
| Chemical Properties | Back Directory | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly) | [form ]
Oil | [color ]
Clear Colorless | [InChIKey]
PLBFDNDNLXVKNK-MHDHNRKVNA-N | [SMILES]
[C@@H]1(OCC2C=CC=CC=2)[C@@H](OCC2C=CC=CC=2)O[C@H](COCC2=CC=CC=C2)[C@@H]1OCC1C=CC=CC=1 |&1:0,9,19,29,r| |
| Hazard Information | Back Directory | [Chemical Properties]
Low Melting Solid | [Uses]
Phenylmethyl 2,3,4-tris-O-(phenylmethyl)-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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