100638-83-3 Usage
Uses
Used in Pharmaceutical Synthesis:
Methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O--α-D-glucopyranoside is used as an intermediate in the synthesis of 2,6-Diamino-2,3,6-trideoxy-D-ribo-Hexose Dihydrochloride (D416795). methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O--α-D-glucopyranoside is a degradent of Tobramycin (T524000), a single-factor antibiotic that is part of the aminoglycosidic antibiotic complex produced by Streptomyces tenebrarius. It is utilized for its antibacterial properties, contributing to the development of new antibiotics to combat bacterial infections.
Used in Antibacterial Applications:
In the pharmaceutical industry, methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O--α-D-glucopyranoside is used as a key component in the development of antibiotics. Its role in the synthesis of Tobramycin-related compounds highlights its importance in creating new antibacterial agents to address the growing issue of antibiotic resistance. The compound's unique structure allows for the exploration of novel drug candidates with improved efficacy and reduced side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 100638-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,3 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100638-83:
(8*1)+(7*0)+(6*0)+(5*6)+(4*3)+(3*8)+(2*8)+(1*3)=93
93 % 10 = 3
So 100638-83-3 is a valid CAS Registry Number.
100638-83-3Relevant academic research and scientific papers
Further Aspects of the Reduction of Dithiocarbonates with Tributyltin Hydride and Deuteride
Conway, Richard J.,Nagel, Jennifer P.,Stick, Robert V.,Tilbrook, D. Matthew G.
, p. 939 - 945 (2007/10/02)
The reduction of 1,2:5,6-di-O-isopropylidene-3-O-(methylthio)thiocarbonyl-β-D-idose, -talose, and -(3-(2H))talose with tributyltin hydride and deuteride leads to the deoxy sugar and some deuteriumcontaining deoxy sugars.A modification of the normal procedure allows for reduction with tributyltin hydride generated in situ.As well, the reduction of some dithiocarbonates derived from glycosides of N-acetyl-D-glucosamine allows to a variety of dideoxy and trideoxy sugars.
