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CAS RN: 100491-29-0 | Product Number: E1180
Ethyl 7-Chloro-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate
Purity: >98.0%(HPLC)(N)
Synonyms:
- 7-Chloro-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic Acid Ethyl Ester
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days | Quantity |
---|---|---|---|---|
5G |
S$49.50
|
6 | 1 |
|
25G |
S$141.00
|
8 | 19 |
|
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* The storage conditions are subject to change without notice.
Product Number | E1180 |
Purity / Analysis Method | >98.0%(HPLC)(N) |
Molecular Formula / Molecular Weight | C__1__7H__1__0ClF__3N__2O__3 = 382.72 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 100491-29-0 |
Reaxys Registry Number | 4766094 |
PubChem Substance ID | 253661440 |
MDL Number | MFCD01863285 |
Specifications
Appearance | White to Almost white powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(with Total Nitrogen) | min. 98.0 % |
Melting point | 213.0 to 217.0 °C |
Properties (reference)
Melting Point | 215 °C |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H317 : May cause an allergic skin reaction. H411 : Toxic to aquatic life with long lasting effects. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P261 : Avoid breathing dust/ fume/ gas/ mist/ vapors/ spray. P273 : Avoid release to the environment. P272 : Contaminated work clothing should not be allowed out of the workplace. P280 : Wear protective gloves. P302 + P352 : IF ON SKIN: Wash with plenty of water. P391 : Collect spillage. P362 + P364 : Take off contaminated clothing and wash it before reuse. P333 + P313 : If skin irritation or rash occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
UN Number | UN3077 |
Class | 9 |
Packing Group | III |
H.S.code* | 2933.99-000 |
Application
The Synthesis of Fluoroquinolone Antibiotics
This compound has previously been converted into tosufloxacin [T2506] by reaction with 3-acetamidopyrrolidine [A1108]. To this day, it has been widely used for the synthesis of fluoroquinolone antibiotics such as trovafloxacin.
References
- Synthesis and structure-activity relationships of new arylfluoronaphthyridine antibacterial agents
- Preparation and in vitro and in vivo evaluation of quinolones with selective activity against Gram-positive organisms
- Synthesis of (1α,5α,6α)-6-amino-3-azabicyclo[3.1.0]hexane, a novel achiral diamine
- Diastereoselective syntheses of N-protected derivatives of 1α,5α,6β-6-amino-3-azabicyclo[3.1.0]hexane. A route to trovafloxacin 6β-diastereomer
- Synthesis of trovafloxacin using various (1α,5α,6α)-3-azabicyclo[3.1.0]hexane derivatives
PubMed Literature
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