24758-68-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-phenylhydrazinyl)hexose is used as a potential therapeutic agent for diabetes management due to its ability to inhibit alpha-amylase, an enzyme involved in carbohydrate breakdown. By inhibiting this enzyme, it may help regulate blood sugar levels and provide a novel approach to treating diabetes and related metabolic disorders.
Used in Research and Development:
1-(2-phenylhydrazinyl)hexose serves as a valuable tool in the research and development of new drugs and therapies. Its role in inhibiting alpha-amylase makes it a promising candidate for studying the mechanisms of carbohydrate metabolism, which can lead to the development of innovative treatments for diabetes and other metabolic conditions.
Used in Drug Design and Development:
1-(2-phenylhydrazinyl)hexose's potential as an alpha-amylase inhibitor also makes it a useful component in the design and development of new drugs aimed at managing blood sugar levels. Its unique structure and properties can be leveraged to create novel drug candidates that target specific metabolic pathways and offer improved treatment options for patients with diabetes and other related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 24758-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,5 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24758-68:
(7*2)+(6*4)+(5*7)+(4*5)+(3*8)+(2*6)+(1*8)=137
137 % 10 = 7
So 24758-68-7 is a valid CAS Registry Number.
24758-68-7Relevant academic research and scientific papers
MAOS of D-gluconic acid, D-glucono-1,4- and 1,5-lactones, esters, hydrazides, and benzimidazoles thereof
El Ashry,Awad,Abdel Hamid,Atta
, p. 329 - 338 (2008/02/12)
Microwave-assisted organic synthesis (MAOS) of D-gluconic acid can be efficiently done by oxidation of D-glucose with bromine water, upon irradiation with microwave (MW). It was also used for the conversion of D-gluconic acid to ethyl D-gluconate, D-glucono-1,4- and 1,5-lactones, gluconyl hydrazide, and gluconyl phenylhydrazide in yields comparable to those obtained by conventional methods, but in much shorter times. A convenient microwave-mediated condensation of D-gluconic acid with o-phenylenediamines provided the respective acyclonucleoside benzimidazole in short time and good yield.
