2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura

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2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura manufacturers

2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura Basic information
Product Name:2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura
Synonyms:[(2R,3R,4S,5R)-3,4-dibenzoyloxy-5-bromooxolan-2-yl]methyl benzoate;2,3,5-tri-o-benzoyl-α-d-arabinofuranosyl bromide;α-D-Arabinofuranosyl bromide, 2,3,5-tribenzoate;2,3,5-Tri-O-benzoyl-α-D-arabinosyl bromide;2,3,5-Tri-O-benzoyl-α-D-brominated arabinose;2-[(2S,3S,4S,5S)-3,4-Dibenzoyl-5-bromo-3,4-dihydroxyoxolan-2-yl]-2-hydroxy-1-phenylethan-1-one;(2R,3R,4S,5R)-2-((Benzoyloxy)methyl)-5-bromotetrahydrofuran-3,4-diyl dibenzoate;2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura
CAS:4348-68-9
MF:C26H21BrO7
MW:525.35
EINECS:
Product Categories:Carbohydrate Synthesis;Monosaccharides;Specialty Synthesis
Mol File:4348-68-9.mol
2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura Structure
2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura Chemical Properties
Boiling point 611.4±55.0 °C(Predicted)
density 1.49±0.1 g/cm3(Predicted)
storage temp. 2-8°C
BRN 98941
Safety Information
WGK Germany 3
3-10
MSDS Information
2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura Usage And Synthesis
Uses2,3,5-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
2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura Preparation Products And Raw materials
Raw materialsD-(-)-Arabinose
Tag:2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura(4348-68-9) Related Product Information
5-Bromopentyl acetate 2 3 5-Tri-O-benzoyl-alpha-D-arabino-fura Benzyl 5-bromopentyl ether (2-Acetoxyethoxy)-methyl bromide Benzyl 3-bromopropyl ether Benzyl 2-bromoethyl ether (S)-3-Bromo-1,2-propanediol 2-Bromoethyl benzoate