33993-25-8 Usage
Description
2-Naphthyl-beta-D-galactopyranoside is a beta-D-galactoside with a 2-naphthyl substituent at the anomeric position. It is a white solid and is commonly used in various applications due to its unique chemical properties.
Uses
Used in Chemical and Pharmaceutical Industry:
2-Naphthyl-beta-D-galactopyranoside is used as a substrate for the detection and quantification of galactosidases, which are enzymes that catalyze the hydrolysis of galactosides. This application is particularly important in the study of enzyme kinetics, enzyme inhibition, and the development of new drugs targeting these enzymes.
Used in Research and Development:
In the field of research and development, 2-Naphthyl-beta-D-galactopyranoside is used as a model compound for studying the interactions between carbohydrates and proteins. This is crucial for understanding the molecular mechanisms of various biological processes, such as cell adhesion, cell signaling, and immune response.
Used in Analytical Chemistry:
2-Naphthyl-beta-D-galactopyranoside is employed as a reference compound in the development and validation of analytical methods for the detection and quantification of carbohydrates. Its unique chemical properties make it an ideal candidate for the calibration of instruments and the establishment of standard curves in various analytical techniques.
Used in Material Science:
In material science, 2-Naphthyl-beta-D-galactopyranoside can be used as a building block for the synthesis of novel carbohydrate-based materials with potential applications in areas such as drug delivery, sensors, and biocompatible coatings.
Used in Biotechnology:
2-Naphthyl-beta-D-galactopyranoside is utilized as a reporter molecule in the field of biotechnology, particularly in the development of biosensors and the study of enzyme activity. Its ability to produce a colorimetric or fluorescent signal upon interaction with specific enzymes makes it a valuable tool for monitoring enzymatic reactions in real-time.
Check Digit Verification of cas no
The CAS Registry Mumber 33993-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,9 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33993-25:
(7*3)+(6*3)+(5*9)+(4*9)+(3*3)+(2*2)+(1*5)=138
138 % 10 = 8
So 33993-25-8 is a valid CAS Registry Number.
33993-25-8Relevant articles and documents
Hierarchical Self-Assembly of a Water-Soluble Organoplatinum(II) Metallacycle into Well-Defined Nanostructures
Datta, Sougata,Saha, Manik Lal,Lahiri, Nabajit,Yu, Guocan,Louie, Janis,Stang, Peter J.
, p. 7020 - 7023 (2018)
A water-soluble metallosupramolecular hexagon containing pendant methyl viologen (MV) and trimethylammonium units at the vertices has been synthesized via an organoplatinum(II) pyridyl coordination-driven self-assembly reaction. The MV units of the metallacycle were further utilized in the formation of a heteroternary complex with cucurbit[8]uril and a galactose-functionalized naphthalene derivative, yielding a metallacycle-cored carbohydrate cluster that was subsequently ordered into nanospheres and tapes, depending upon the concentration.
Solution and Solid-Phase Stereocontrolled Synthesis of 1,2-cis-Glycopyranosides with Minimally Protected Glycopyranosyl Donors Catalyzed by BF3-N,N-Dimethylformamide Complex
St-Pierre, Gabrielle,Hanessian, Stephen
supporting information, p. 3106 - 3109 (2016/07/14)
Methods are described for the stereoselective synthesis of 1,2-cis glycopyranosides in the d-galacto, d-gluco, and 2-azido-2-deoxy-d-glucopyranoside series utilizing minimally protected (3-bromo-2-pyridyloxy) β-d-glycopyranosyl donors in the presence of BF3-N,N-dimethylformamide (DMF) as a catalyst and a variety of alcohol acceptors relying on the "remote activation concept". Precursors to antifreeze glycopeptide components are synthesized in excellent yields and high α/β ratios. The method is adaptable to one-pot sequential glycosidation as well as to solid-supported synthesis giving access to diverse sets of minimally protected α-d-glycopyranosides as major products.
