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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)
Chemical Substance Law (ENCS):   5-6439
Synonyms:
  • 7-Chloro-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic Acid Ethyl Ester
Product Documents:
5G
¥3,600
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25G
¥10,300
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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 Pictogram 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:
Chemical Substance Law (ENCS) 5-6439
Transport Information:
UN Number UN3077
Class 9
Packing Group III
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


PubMed Literature


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