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6-Bromo-2-naphthyl α-D-galactopyranoside

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6-Bromo-2-naphthyl α-D-galactopyranoside manufacturers

6-Bromo-2-naphthyl α-D-galactopyranoside Basic information
Product Name:6-Bromo-2-naphthyl α-D-galactopyranoside
Synonyms:6-BROMO NAPHTHYL GALACTOPYRANOSIDE;6-BROMO-2-NAPHTHYL-A-D-GALACTOPYRANOSIDE;6-BROMO-2-NAPHTHYL-ALPHA-D-GALACTOPYRANOSIDE;2-(6-BROMONAPHTHYL)-ALPHA-D-GALACTOPYRANOSIDE;BR-NAP-ALPHA-D-GAL;BROMO-2-NAPHTHYL-A-D-GALACTOPYRANOSIDE, 6-;6-Bromo-2-Naphthyl-Alpha-D-Galactopyran-;(6-Bromo-2-naphthalenyl)α-D-galactopyranoside
CAS:25997-59-5
MF:C16H17BrO6
MW:385.21
EINECS:247-398-4
Product Categories:Substrates;13C & 2H Sugars;Carbohydrates & Derivatives;substrate
Mol File:25997-59-5.mol
6-Bromo-2-naphthyl α-D-galactopyranoside Structure
6-Bromo-2-naphthyl α-D-galactopyranoside Chemical Properties
Melting point 225°C
Boiling point 609℃
density 1.698
Fp 322℃
solubility soluble in Methanol, Water
Safety Information
HS Code 29389090
MSDS Information
6-Bromo-2-naphthyl α-D-galactopyranoside Usage And Synthesis
Uses6-Bromo-2-naphthyl α-D-galactopyranoside can be acted as a useful reagent for determination of alpha-D-Galactosidase activity.
DefinitionChEBI: An alpha-D-galactoside having a 6-bromo-2-naphthyl substituent at the anomeric position.
Purification MethodsIt is prepared from penta-O-acetyl-D-galactoside, 6-bromo-2naphthol and ZnCl2. The resulting tetra-acetate (2g) is hydrolysed by dissolving in 0.3N KOH (100mL) and heating until the solution is clear, then filtering and cooling to give colourless crystals of the -isomer which are collected and recrystallised twice from hot MeOH. The high specific rotation is characteristic of the isomer. The tetraacetate has m 155-156o, [] D 20 +60o (c 1, CHCl3) [Dey & Pridham Biochem J 115 47 1969] [reported m 75-85o, [] D 24 +94o (c 1.3, dioxane), Monis et al. J Histochem Cytochem 11 653 1963]. [Beilstein 17 IV 2972.]
6-Bromo-2-naphthyl α-D-galactopyranoside Preparation Products And Raw materials
Tag:6-Bromo-2-naphthyl α-D-galactopyranoside(25997-59-5) Related Product Information
Methyl alpha-D-fucopyranoside 2-Bromo-6-butoxynaphthalene Ph-alpa-D-Gal 2-(2-Naphthoxy)ethanol 2-Bromo-6-methoxynaphthalene METHYL-ALPHA-D-GALACTOPYRANOSIDE 2-Bromonaphthalene D-Galactose 6-Bromo-2-naphthyl α-D-galactopyranoside 6-Bromo-2-naphthol 6-ETHOXY-2-BROMONAPHTHALENE