Name | 4-Fluoro-2-methoxyaniline |
Synonyms | o-Anisidine, 4-fluoro- 2-Amino-5-fluoroanisole 2-Methoxy-4-fluoroaniline 4-FLUORO-2-METHOXYANILINE 4-Fluoro-2-methoxyaniline 4-Fluoro-2-MethoxybenzenaMine 4-Fluoro-2-methoxy-phenylamine benzenamine, 4-fluoro-2-methoxy- 4-Fluoro-o-anisidine, 2-Amino-5-fluoroanisole 2-AMino-5-fluoroanisole[4-Fluoro-2-Methoxyaniline] |
CAS | 450-91-9 |
EINECS | 814-457-6 |
InChI | InChI=1/C7H8FNO/c1-10-7-4-5(8)2-3-6(7)9/h2-4H,9H2,1H3 |
Molecular Formula | C7H8FNO |
Molar Mass | 141.14 |
Density | 1.176±0.06 g/cm3 (20 ºC 760 Torr) |
Boling Point | 215℃ (756 Torr) |
Flash Point | 79.5±21.8℃ |
Vapor Presure | 0.22mmHg at 25°C |
Appearance | Solid |
Color | Colorless to Brown |
pKa | 4.60±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Refractive Index | 1.5400 to 1.5440 |
MDL | MFCD00077536 |
UN IDs | 2810 |
Hazard Class | 6.1 |
Packing Group | Ⅲ |
Uses | 4-fluoro-2-o-methoxyaniline is a useful synthetic intermediate, which can be used to prepare ortho-substituted phenylurea as 5-Hydroxytryptamine (5-HT3) receptor antagonist, is also used to synthesize hydroxamic acid and its prodrugs as inhibitors of the light chain of botulinum neurotoxin A. |
Synthesis method | Using 4-fluoro-2-o-methoxynitrobenzene as the starting material, the target compound 4-fluoro-2-o-methoxyaniline is prepared by hydrogenation reduction reaction. The synthesis reaction formula is as follows: |