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| | 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 | | EINECS: | | | Product Categories: | 13C & 2H Sugars;Carbohydrates & Derivatives | | Mol File: | 40983-95-7.mol |  |
| | 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) |
| | 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-mannopyranoside Preparation Products And Raw materials |
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