| Company Name: |
J & K SCIENTIFIC LTD.
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18210857532; 18210857532 |
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jkinfo@jkchemical.com |
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Product Name:BroMo 2,4,6-Tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl -b-D-glucopyranosyl)-α-D-glucopyranoside
CAS:23202-66-6
Package:50Mg,5Mg
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| Company Name: |
Chemsky（shanghai）International Co.,Ltd.
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| Tel: |
021-50135380 |
| Email: |
shchemsky@sina.com |
| Products Intro: |
Product Name:BroMo 2,4,6-Tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl -b-D-glucopyranosyl)-α-D-glucopyranoside
CAS:23202-66-6
Purity:98%
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| | 4,5,7-TRI-O-ACETYL-2,6-ANHYDRO-3-DEOXY-D-LYXO-HEPT-2-ENONONITRILE Basic information |
| Product Name: | 4,5,7-TRI-O-ACETYL-2,6-ANHYDRO-3-DEOXY-D-LYXO-HEPT-2-ENONONITRILE | | Synonyms: | 2,4,6-Tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-a-D-glucopyranosylbromide;Bromo 2,4,6-Tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl -b-D-glucopyranosyl)-α-D-glucopyranoside;3-O-(2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl)-α-D-glucopyranosyl BroMide Triacetate;α-D-Glucopyranosyl bromide, 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-, 2,4,6-triacetate;(2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(((2R,3R,4S,5R,6R)-3,5-diacetoxy-2-(acetoxymethyl)-6-bromotetrahydro-2H-pyran-4-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate;1-Bromo-2,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-alpha-D-glucopyranoside | | CAS: | 23202-66-6 | | MF: | C26H35BrO17 | | MW: | 699.45 | | EINECS: | | | Product Categories: | Oligosaccharides | | Mol File: | 23202-66-6.mol |  |
| | 4,5,7-TRI-O-ACETYL-2,6-ANHYDRO-3-DEOXY-D-LYXO-HEPT-2-ENONONITRILE Chemical Properties |
| Melting point | 148-150°C | | Boiling point | 659.5±55.0 °C(Predicted) | | density | 1.47±0.1 g/cm3(Predicted) | | solubility | Dichloromethane, Ether, Ethyl Acetate, Methanol | | form | Solid | | color | White Crystalline |
| | 4,5,7-TRI-O-ACETYL-2,6-ANHYDRO-3-DEOXY-D-LYXO-HEPT-2-ENONONITRILE Usage And Synthesis |
| Chemical Properties | White Crystalline Solid | | Uses | 2,3,4,6-Tetra-O-acetyl-β-D-glucose (Acetobromolaminaribiose) 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 |
| | 4,5,7-TRI-O-ACETYL-2,6-ANHYDRO-3-DEOXY-D-LYXO-HEPT-2-ENONONITRILE Preparation Products And Raw materials |
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