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

6-Bromo-2-naphthyl α-D-galactopyranoside
  • CAS No.:25997-59-5

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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Other grades of this product :
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 Chemical Properties
Melting point 225°C
Boiling point 609℃
density 1.698
Fp 322℃
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

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