logo
Home  > 7H-Pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid,9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-,hydrochloride, (±)-

AX16066

118120-51-7 | 7H-Pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid,9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-,hydrochloride, (±)-

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $355.00 $249.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AX16066
Chemical Name: 7H-Pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid,9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-,hydrochloride, (±)-
CAS Number: 118120-51-7
Molecular Formula: C18H21ClFN3O4
Molecular Weight: 397.8284
MDL Number: MFCD06410951
SMILES: CC1COC2=C3N1C=C(C(=O)C3=CC(=C2N4CCN(CC4)C)F)C(=O)O.Cl

 

Computed Properties
Complexity: 634  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 27  
Hydrogen Bond Acceptor Count: 8  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  

 

 

Upstream Synthesis Route
  • Ofloxacin hydrochloride, a fluoroquinolone antibiotic, plays a crucial role in chemical synthesis due to its diverse applications. With its broad-spectrum antibacterial properties, Ofloxacin hydrochloride is utilized in the synthesis of new pharmaceutical compounds and drugs. Specifically, it serves as a key building block in the creation of novel antibacterial agents and antimicrobial formulations. In addition, its chemical structure and reactivity make it a valuable component in the development of specialized drug delivery systems, promoting targeted and efficient drug release mechanisms. Furthermore, Ofloxacin hydrochloride's versatile properties enable its incorporation into various chemical reactions, enabling the synthesis of advanced materials with enhanced therapeutic benefits. Its significance in chemical synthesis extends beyond traditional pharmaceutical applications, contributing to the advancement of drug discovery and development processes.
Literature
FEATURED PRODUCTS