124476-99-9 Usage
Uses
Used in Organic Synthesis:
Phenyl 3,4-O-(1-methylethylidene)-1-thio-beta-D-galactopyranoside diacetate is used as a key intermediate in the synthesis of various organic compounds, particularly those involving complex carbohydrate structures. Its unique structural features make it a valuable building block for creating novel molecules with potential applications in pharmaceuticals and materials science.
Used in Biochemical Research:
In the field of biochemistry, Phenyl 3,4-O-(1-methylethylidene)-1-thio-beta-D-galactopyranoside diacetate serves as a research tool for studying enzyme mechanisms and protein interactions. Its ability to bind with enzymes and proteins allows researchers to probe the structure and function of these biomolecules, contributing to a deeper understanding of biological processes and the development of new therapeutic agents.
Used in Pharmaceutical Development:
Phenyl 3,4-O-(1-methylethylidene)-1-thio-beta-D-galactopyranoside diacetate is employed as a potential lead compound in the development of new pharmaceuticals. Its unique structure and interactions with biological targets make it a promising candidate for the treatment of various diseases, including those involving carbohydrate-related pathways and enzyme inhibition.
Used in Material Science:
In material science, Phenyl 3,4-O-(1-methylethylidene)-1-thio-beta-D-galactopyranoside diacetate is utilized for the development of advanced materials with specific properties. Its incorporation into polymers and other materials can lead to the creation of novel materials with improved characteristics, such as enhanced stability, biocompatibility, or specific binding properties.
Used in Analytical Chemistry:
Phenyl 3,4-O-(1-methylethylidene)-1-thio-beta-D-galactopyranoside diacetate is also used in analytical chemistry as a reference compound or a standard for the development and validation of analytical methods. Its unique structure and properties make it suitable for calibrating instruments and ensuring the accuracy of measurements in various chemical analyses.
Check Digit Verification of cas no
The CAS Registry Mumber 124476-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,7 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124476-99:
(8*1)+(7*2)+(6*4)+(5*4)+(4*7)+(3*6)+(2*9)+(1*9)=139
139 % 10 = 9
So 124476-99-9 is a valid CAS Registry Number.
124476-99-9Relevant academic research and scientific papers
PREPARATION OF PYRANOID GLYCAL DERIVATIVES FROM PHENYL THIOGLYCOSIDES AND GLYCOSYL PHENYL SULPHONES
Fernandez-Mayoralas, Alfonso,Marra, Alberto,Trumtel, Michel,Veyrieres, Alain,Sinay, Pierre
, p. 81 - 96 (2007/10/02)
Phenyl thioglycopyranosides with various protecting groups (acetal, ether, ester) underwent reductive lithiation at C-1, followed by rapid elimination of the 2-substituent, when treated with lithium naphthalenide in tetrahydrofuran at low temperature.Thus
