77392-66-6 Usage
Uses
Used in Organic Synthesis:
(2-Ethyl 2,3,4-Tri-O-acetyl--D-glucopyranoside) Uronate is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for selective reactions and functional group manipulations, making it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2-Ethyl 2,3,4-Tri-O-acetyl--D-glucopyranoside) Uronate is used as a starting material for the synthesis of drug candidates with potential therapeutic applications. Its ability to be selectively modified and functionalized makes it an attractive candidate for the development of new drugs with improved pharmacological properties.
Used in Research and Development:
(2-Ethyl 2,3,4-Tri-O-acetyl--D-glucopyranoside) Uronate is also utilized in research and development settings for the study of carbohydrate chemistry, enzymatic reactions, and the development of new synthetic methodologies. Its unique structure and reactivity provide valuable insights into the fundamental aspects of organic chemistry and contribute to the advancement of scientific knowledge in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 77392-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,9 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77392-66:
(7*7)+(6*7)+(5*3)+(4*9)+(3*2)+(2*6)+(1*6)=166
166 % 10 = 6
So 77392-66-6 is a valid CAS Registry Number.
77392-66-6Relevant academic research and scientific papers
ELECTROCHEMICAL METHODS AND COMPOUNDS FOR THE DETECTION OF ENZYMES
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Page/Page column 49; 50, (2016/04/26)
Disclosed are compositions and methods for the electrochemical detection of enzymes, such as enzymes that are indicative of disease, disorders, or pathogens, such as viruses, bacteria, and fungi, or other disorders. These methods can be used in point-of- care diagnostic assays for the detection of disease, disorder, or pathogen (e.g., to identify the strain of pathogen infecting a patient in a healthcare setting). The electrochemical methods described herein can also be used to assess the susceptibility of a pathogen to an antipathogen drug. Also provided are probes suitable for use in conjunction with the methods described herein.
Koenigs-Knorr reaction of fusel alcohols with methyl (1-bromo-2,3,4-tri-O- acetyl-α-d-glucopyranosid)uronate leading to the protected alkyl glucuronides - Crystal structures and high resolution 1H and 13C NMR data
M?nch, Bettina,Gebert, Antje,Emmerling, Franziska,Becker, Roland,Nehls, Irene
experimental part, p. 186 - 190 (2012/05/04)
Crystal structures and high resolution 1H and 13C NMR spectral data for methyl (alkyl 2,3,4-tri-O-acetyl-β-d-glucopyranosid) uronates (alkyl = methyl, ethyl, n-propyl, i-propyl, n-butyl, sec-butyl, i-butyl, n-pentyl, 2-methyl-1-butyl and 3-methyl-1-butyl) are presented.
