951163-60-3 Usage
Description
Butanedioicacid,2-hydroxy-,compd.with7-[(3S,5S)-3-amino-5-methyl-1-piperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylicacid is a complex organic compound that belongs to the class of quinolone antibacterial agents. It is characterized by its unique molecular structure, which includes a butanedioic acid moiety, a 2-hydroxy group, and a cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid component. Butanedioicacid,2-hydroxy-,compd.with7-[(3S,5S)-3-amino-5-methyl-1-piperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylicacid exhibits potent antibacterial properties and is used in the treatment of various infections.
Uses
Used in Pharmaceutical Industry:
Butanedioicacid,2-hydroxy-,compd.with7-[(3S,5S)-3-amino-5-methyl-1-piperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylicacid is used as an antibacterial agent for the treatment of pneumonia and oral treatment of diabetic foot ulcer skin infections. Its potent antibacterial activity makes it an effective treatment option for these conditions.
Used in Research and Development:
Butanedioicacid,2-hydroxy-,compd.with7-[(3S,5S)-3-amino-5-methyl-1-piperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylicacid is also used in research and development for the discovery of new antibacterial drugs. Its unique structure and properties make it a valuable tool for studying the mechanisms of action and resistance to quinolone antibiotics, which can contribute to the development of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 951163-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,1,6 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 951163-60:
(8*9)+(7*5)+(6*1)+(5*1)+(4*6)+(3*3)+(2*6)+(1*0)=163
163 % 10 = 3
So 951163-60-3 is a valid CAS Registry Number.
951163-60-3Relevant articles and documents
Hydride reduction process for preparing quinolone intermediates
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Page/Page column 8-9, (2008/06/13)
Hydride process for making acyclic diol intermediates from cyclic intermediates, useful in antibacterial quinolone synthesis.
