4,6-O-Benzylidene-N-Boc-1,5-imino-D-glucitol
4,6-O-Benzylidene-N-Boc-1,5-imino-D-glucitol Basic information
- Product Name:
- 4,6-O-Benzylidene-N-Boc-1,5-imino-D-glucitol
- Synonyms:
-
- 4,6-O-Benzylidene-N-Boc-1,5-imino-D-glucitol
- [2R-(2α,4aα,7α,8β,8aβ)]-Hexahydro-7,8-dihydroxy-2-phenyl-5H-1,3-dioxino[5,4-b]pyridine-5-carboxylic Acid 1,1-DiMethylethyl Ester
- 5H-1,3-Dioxino[5,4-b]pyridine-5-carboxylic acid, hexahydro-7,8-dihydroxy-2-phenyl-, 1,1-dimethylethyl ester, [2R-(2α,4aα,7α,8β,8aβ)]- (9CI)
- CAS:
- 133697-16-2
- MF:
- C18H25NO6
- MW:
- 351.39
- Product Categories:
-
- Carbohydrates & Derivatives
- Mol File:
- 133697-16-2.mol
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4,6-O-Benzylidene-N-Boc-1,5-imino-D-glucitol Chemical Properties
- Melting point:
- 162-164°C
- solubility
- soluble in Dichloromethane, Methanol
- form
- Solid
- color
- White
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4,6-O-Benzylidene-N-Boc-1,5-imino-D-glucitol Usage And Synthesis
Chemical Properties
White Solid
Uses
4,6-O-Benzylidene-N-(tert-butoxycarbonyl)-1,5-imino-D-glucitol 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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