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Home  > 3-Quinolinecarboxylic acid,1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-,hydrochloride

AX19896

112732-17-9 | 3-Quinolinecarboxylic acid,1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-,hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $59.00 $41.00 -   +
5g 95% in stock $139.00 $97.00 -   +
10g 95% in stock $234.00 $164.00 -   +
25g 95% in stock $547.00 $383.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AX19896
Chemical Name: 3-Quinolinecarboxylic acid,1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-,hydrochloride
CAS Number: 112732-17-9
Molecular Formula: C19H23ClFN3O3
Molecular Weight: 395.8556
MDL Number: MFCD00792463
SMILES: CCN1CCN(CC1)c1cc2c(cc1F)c(=O)c(cn2C1CC1)C(=O)O.Cl

 

Computed Properties
Complexity: 613  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 27  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • Enrofloxacin HCl is a widely used antibiotic in the veterinary field, known for its effectiveness in treating bacterial infections in animals. However, beyond its use in medicine, Enrofloxacin HCl also plays a crucial role in chemical synthesis processes. In the realm of organic chemistry, Enrofloxacin HCl can serve as a valuable reagent for the synthesis of various compounds.Its chemical structure and properties make it a versatile building block for the creation of complex molecules, particularly in the pharmaceutical industry. Enrofloxacin HCl's fluorine atom and other functional groups present opportunities for selective reactions and derivatization, allowing chemists to manipulate its structure to generate novel drug candidates or fine chemicals.Furthermore, the presence of the HCl salt form of Enrofloxacin enhances its solubility and stability in aqueous environments, making it a desirable reagent for reactions that require aqueous conditions. This feature expands the range of reactions in which Enrofloxacin HCl can participate, making it a valuable tool in chemical synthesis strategies.In summary, Enrofloxacin HCl's role in chemical synthesis goes beyond its antibiotic properties, showcasing its versatility and significance in the realm of organic chemistry.
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