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| | Methyl-2,3,4-tri-O-benzyl-L-fucopyranose Basic information |
| Product Name: | Methyl-2,3,4-tri-O-benzyl-L-fucopyranose | | Synonyms: | Methyl-2,3,4-tri-O-benzyl-L-fucopyranose,98%;METHYL-2,3,4-TRI-O-BENZYL-BETA-L-FUCOPYRANOSIDE;Methyl2,3,4-tri-O-benzyl-L-fucopyranoside;METHYL-2,3,4-TRI-O-BENZYL-SS-L-FUCOPYRANOSIDE;L-Galactopyranoside, methyl 6-deoxy-2,3,4-tris-O-(phenylmethyl)-;Methyl-2,3,4-tri-O-benzyl-L-fucopyranose | | CAS: | 67576-77-6 | | MF: | C28H32O5 | | MW: | 448.55 | | EINECS: | | | Product Categories: | Carbohydrates & Derivatives | | Mol File: | 67576-77-6.mol |  |
| | Methyl-2,3,4-tri-O-benzyl-L-fucopyranose Chemical Properties |
| Boiling point | 517.26°C (rough estimate) | | density | 1.0792 (rough estimate) | | refractive index | 1.5400 (estimate) |
| Safety Statements | 24/25 | | HS Code | 29400000 |
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ACROS
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| | Methyl-2,3,4-tri-O-benzyl-L-fucopyranose Usage And Synthesis |
| Chemical Properties | Yellow Oil | | Uses | Methyl 6-deoxy-2,3,4-tris-O-(phenylmethyl)-L-galactopyranoside 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 |
| | Methyl-2,3,4-tri-O-benzyl-L-fucopyranose Preparation Products And Raw materials |
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