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Home  > 3-Quinolinecarboxylic acid, 1-cyclopropyl-7-[(3R,5S)-3,5-dimethyl-1-piperazinyl]-5,6,8-trifluoro-1,4-dihydro-4-oxo-, rel-

AA11693

113617-63-3 | 3-Quinolinecarboxylic acid, 1-cyclopropyl-7-[(3R,5S)-3,5-dimethyl-1-piperazinyl]-5,6,8-trifluoro-1,4-dihydro-4-oxo-, rel-

Packsize Purity Availability Price Discounted Price    Quantity
100mg 99% in stock $38.00 $26.00 -   +
250mg 99% in stock $53.00 $37.00 -   +
1g 99% in stock $129.00 $90.00 -   +
5g 99% in stock $442.00 $309.00 -   +

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*All prices are in USD.

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Description
Catalog Number: AA11693
Chemical Name: 3-Quinolinecarboxylic acid, 1-cyclopropyl-7-[(3R,5S)-3,5-dimethyl-1-piperazinyl]-5,6,8-trifluoro-1,4-dihydro-4-oxo-, rel-
CAS Number: 113617-63-3
Molecular Formula: C19H20F3N3O3
Molecular Weight: 395.3756
MDL Number: MFCD00864858
SMILES: C[C@@H]1N[C@H](C)CN(C1)c1c(F)c(F)c2c(c1F)n(cc(c2=O)C(=O)O)C1CC1
NSC Number: 758614

 

Computed Properties
Complexity: 691  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 28  
Hydrogen Bond Acceptor Count: 9  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 3  
XLogP3: 0.9  

 

 

Upstream Synthesis Route 
  • Orbifloxacin, a synthetic fluoroquinolone antibiotic, serves as a valuable reagent in chemical synthesis due to its unique molecular structure and pharmacological properties. In the realm of organic chemistry, Orbifloxacin can be utilized as a building block or precursor in the production of various pharmaceutical compounds. Its quinolone scaffold, containing a fluorine atom at position 6, imparts specific reactivity and interactions that are advantageous in the creation of novel molecules. When incorporated into synthesis routes, Orbifloxacin can introduce specific functional groups, stereochemistry, or pharmacophores that are essential for designing bioactive compounds with targeted therapeutic effects. Furthermore, its broad-spectrum antimicrobial activity can be exploited in medicinal chemistry research to explore structure-activity relationships and develop new drug candidates with enhanced efficacy and safety profiles. Overall, Orbifloxacin's role in chemical synthesis extends beyond its antibiotic properties, offering a versatile tool for molecular design and drug discovery endeavors.
Literature
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