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CAS RN: 68077-26-9 | Product Number: C2897
7-Chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic Acid
Purity: >98.0%(T)(HPLC)
Synonyms:
Product Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
1G |
£27.00
|
1 | 27 |
|
5G |
£124.00
|
1 | 37 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Product Number | C2897 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__1__2H__9ClFNO__3 = 269.66 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 68077-26-9 |
Reaxys Registry Number | 413730 |
PubChem Substance ID | 253661359 |
MDL Number | MFCD00792459 |
Specifications
Appearance | White to Orange to Green powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Neutralization titration) | min. 98.0 % |
NMR | confirm to structure |
Properties (reference)
Melting Point | 284 °C |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. H412 : Harmful to aquatic life with long lasting effects. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
HS Number | 2933499090 |
Application
The Synthesis of Fluoroquinolone Antibiotics
This compound has previously been converted into norfloxacin [N0817] by the reaction with piperazine. To this day, it has been widely used for the synthesis of fluoroquinolone antibiotics.
References
- Structure-activity relationships of antibacterial 6,7- and 7,8-disubstituted 1-alkyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acids
- New structure-activity relationships of the quinolone antibacterials using the target enzyme. The development and application of a DNA gyrase assay
- A new short and efficient strategy for the synthesis of quinolone antibiotics
- Synthesis of 6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid derivatives as potential antimicrobial agents
- Hybrid Antibacterials. DNA Polymerase-Topoisomerase Inhibitors
- Discovery of a Novel Series of Quinolone and Naphthyridine Derivatives as Potential Topoisomerase I Inhibitors by Scaffold Modification
PubMed Literature
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