63554-16-5 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
Methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside is used as a research compound for studying its potential as an anticancer, antiviral, and antibacterial agent. Its unique structure and functional groups enable the exploration of structure-activity relationships and the design of new therapeutic agents with improved efficacy and reduced side effects.
Used in Anticancer Applications:
In the field of oncology, methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside is used as a potential anticancer agent. Its potent biological activities make it a promising candidate for the development of new cancer treatments.
Used in Antiviral Applications:
Methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside is also used as a potential antiviral agent, with its unique structure and functional groups offering the possibility of developing new treatments for viral infections.
Used in Antibacterial Applications:
In the field of microbiology, methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside is used as a potential antibacterial agent, with its potent biological activities making it a candidate for the development of new antibiotics to combat bacterial infections.
Check Digit Verification of cas no
The CAS Registry Mumber 63554-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,5 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63554-16:
(7*6)+(6*3)+(5*5)+(4*5)+(3*4)+(2*1)+(1*6)=125
125 % 10 = 5
So 63554-16-5 is a valid CAS Registry Number.
63554-16-5Relevant academic research and scientific papers
Synthesis of spacer-linked tail to tail dimers derived from a conformationally rigid aminodeoxysugar by olefin metathesis
Kirschning, Andreas,Chen, Guang-Wu
, p. 1133 - 1137 (2007/10/03)
The preparation of new tail to tail dimers of bridged aminodeoxysugars 2 and 11 is described. The first key step in the synthesis is the formation of the aminomethyl bridge in the carbohydrate-derived monomer 7 which is achieved by silver promoted ring closure of methyl 3-acetamido-6-bromo-2,3,6- trideoxy α-D-glucoside 6. Secondly, olefin metathesis of the corresponding 4-O-allyl glycoside 9 constitutes a powerful tool for dimerization, which allows synthesis of 1,4-butanediol-linked tail to tail neooligosaccharides 2 and 11.
