86483-48-9 Usage
Description
Ciprofloxacin hydrochloride, also known as Cipro, is a synthetic broad-spectrum antibacterial agent with the chemical formula C17H18FN3O3·HCl·H2O. It belongs to the quinolone class of antibiotics and is characterized by the presence of a fluorine atom at the 6-position, a piperazine moiety at the 7-position, and a cyclopropyl ring at the 1-position. Ciprofloxacin hydrochloride is highly effective against a wide range of bacterial infections and was the drug of choice for combating anthrax.
Uses
Used in Pharmaceutical Industry:
Ciprofloxacin hydrochloride is used as an antibiotic for treating various bacterial infections, including enteritis caused by diarrheogenic Escherichia coli, Vibrio cholerae, Salmonella species, Shigella species, Campylobacter jejuni, Aeromonas species, and Yersinia enterocolitica. Its broad-spectrum activity and high potency make it a valuable asset in the treatment of a wide range of bacterial infections.
Used in Antimicrobial Applications:
Ciprofloxacin hydrochloride is used as an antimicrobial agent for its ability to effectively target and eliminate a variety of bacteria responsible for infections. Its unique chemical structure allows it to penetrate bacterial cell walls and inhibit essential enzymes, ultimately leading to the death of the bacteria and resolution of the infection.
Used in Hospital Settings:
Ciprofloxacin hydrochloride is used as a therapeutic agent in hospital settings for the treatment of severe or life-threatening bacterial infections. Its broad-spectrum activity and high potency make it a preferred choice for treating infections that are resistant to other antibiotics or when the causative bacteria are yet to be identified.
Used in Research and Development:
Ciprofloxacin hydrochloride is used as a research compound for studying the mechanisms of action, resistance, and development of new antibiotics. Its unique chemical structure and broad-spectrum activity provide valuable insights into the design and development of novel antimicrobial agents to combat antibiotic-resistant bacteria.
Check Digit Verification of cas no
The CAS Registry Mumber 86483-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86483-48:
(7*8)+(6*6)+(5*4)+(4*8)+(3*3)+(2*4)+(1*8)=169
169 % 10 = 9
So 86483-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H18FN3O3.ClH/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24;/h7-10,19H,1-6H2,(H,23,24);1H
86483-48-9Relevant articles and documents
An expeditious synthesis of quinolone antibacterials
Heravi, Majid M.,Oskooie, Hossein A.,Motamedi, Radineh,Ghassemzadeh, Mitra
, p. 423 - 426 (2007/10/03)
A facile and rapid synthesis of ciprofloxacin under microwave irradiation is described. The product ciprofloxacin was isolated and the impurity was characterized as the product of substitution of fluorine instead of chlorine in acid 1. Similarly norfloxacin was synthesized.
