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| | 1,2,3,6-Tetra-O-benzyl-b-D-galactopyranoside Basic information |
| Product Name: | 1,2,3,6-Tetra-O-benzyl-b-D-galactopyranoside | | Synonyms: | 1,2,3,6-Tetra-O-benzyl-b-D-galactopyranoside;1,2,3,6-Tetra-O-benzyl-β-D-galactopyranoside;Benzyl 2,3,6-Tri-O-benzyl-β-D-galactopyranoside;Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-D-galactopyranoside;1,2,3,6-Tetra-O-benzyl-beta-D-galactopyranoside;Benzyl 2,3-Di-O-benzyl-4-O-benzoyl-β-D-galactopyranoside, CAS 57783-81-0 | | CAS: | 57783-81-0 | | MF: | C34H36O6 | | MW: | 540.65 | | EINECS: | | | Product Categories: | Carbohydrates & Derivatives | | Mol File: | 57783-81-0.mol |  |
| | 1,2,3,6-Tetra-O-benzyl-b-D-galactopyranoside Chemical Properties |
| Boiling point | 676.1±55.0 °C(Predicted) | | density | 1.22±0.1 g/cm3(Predicted) | | pka | 12.92±0.70(Predicted) |
| | 1,2,3,6-Tetra-O-benzyl-b-D-galactopyranoside Usage And Synthesis |
| Uses | Benzyl 2,3-Di-O-benzyl-4-O-benzoyl-β-D-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 |
| | 1,2,3,6-Tetra-O-benzyl-b-D-galactopyranoside Preparation Products And Raw materials |
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