| Identification | Back Directory | [Name]
2 3 5-TRI-O-BENZOYL-ALPHA-D-ARABINO-FURA | [CAS]
4348-68-9 | [Synonyms]
2 3 5-TRI-O-BENZOYL-ALPHA-D-ARABINO-FURA
2,3,5-Tri-O-benzoyl-α-D-arabinosyl bromide
2,3,5-Tri-O-benzoyl-α-D-brominated arabinose
α-D-Arabinofuranosyl bromide, 2,3,5-tribenzoate
2,3,5-tri-o-benzoyl-α-d-arabinofuranosyl bromide
[(2R,3R,4S,5R)-3,4-dibenzoyloxy-5-bromooxolan-2-yl]methyl benzoate
2-[(2S,3S,4S,5S)-3,4-Dibenzoyl-5-bromo-3,4-dihydroxyoxolan-2-yl]-2-hydroxy-1-phenylethan-1-one | [Molecular Formula]
C26H21BrO7 | [MDL Number]
MFCD03791085 | [MOL File]
4348-68-9.mol | [Molecular Weight]
525.34 |
| Hazard Information | Back Directory | [Uses]
2,3,5-Tri-O-benzoyl-α-D-arabinofuranosyl bromide 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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