4-FLUORO-2-METHOXYANILINE
4-FLUORO-2-METHOXYANILINE Basic information
- Product Name:
- 4-FLUORO-2-METHOXYANILINE
- Synonyms:
-
- 2-Methoxy-4-fluoroaniline
- 4-FLUORO-2-METHOXYANILINE
- 4-Fluoro-2-MethoxybenzenaMine
- o-Anisidine, 4-fluoro-
- 4-Fluoro-2-methoxy-phenylamine
- 4-Fluoro-o-anisidine, 2-Amino-5-fluoroanisole
- 2-AMino-5-fluoroanisole[4-Fluoro-2-Methoxyaniline]
- 2-Amino-5-fluoroanisole
- CAS:
- 450-91-9
- MF:
- C7H8FNO
- MW:
- 141.14
- EINECS:
- 814-457-6
- Product Categories:
-
- API
- Mol File:
- 450-91-9.mol
4-FLUORO-2-METHOXYANILINE Chemical Properties
- Boiling point:
- 215℃ (756 Torr)
- Density
- 1.176±0.06 g/cm3 (20 ºC 760 Torr)
- refractive index
- 1.5400 to 1.5440
- Flash point:
- 79.5±21.8℃
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- form
- Solid
- pka
- 4.60±0.10(Predicted)
- color
- Colorless to Brown
- InChI
- InChI=1S/C7H8FNO/c1-10-7-4-5(8)2-3-6(7)9/h2-4H,9H2,1H3
- InChIKey
- BNRRMRUVYDETQC-UHFFFAOYSA-N
- SMILES
- C1(N)=CC=C(F)C=C1OC
4-FLUORO-2-METHOXYANILINE Usage And Synthesis
Physical Form
Yellow to Orange to Brown Solid or liquid
Application
4-Fluoro-2-methoxyaniline is a useful synthetic intermediate. It is used to prepare ortho-substituted phenylureas as 5-Hydroxytryptamine (5-HT3) receptor antagonists. It is also used to synthesize hydroxamic acids and their prodrugs as inhibitors for Botulinum neurotoxin A light chain.
Synthesis
Using 4-fluoro-2-o-methoxynitrobenzene as the starting material, the target compound 4-fluoro-2-methoxyaniline was prepared by hydrogenation reduction reaction.
References
[1] Patent: US6352993, 2002, B1. Location in patent: Page column 30
[2] Patent: CN106366072, 2017, A. Location in patent: Paragraph 0062; 0063; 0064; 0090; 0091; 0092
[3] Patent: CN106366022, 2017, A. Location in patent: Paragraph 0051; 0052; 0056
[4] Patent: US2011/130415, 2011, A1. Location in patent: Page/Page column 102
[5] Patent: WO2018/207120, 2018, A1. Location in patent: Page/Page column 11; 12
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4-FLUORO-2-METHOXYANILINE(450-91-9)Related Product Information
- 4-FLUORO-2-METHOXYANILINE
- 2-Acetonyloxy-3,4-difluoro nitrobenzene
- Levofloxacin
- Levofloxacin carboxylic acid
- Ipodate Sodium
- Marbofloxacin
- 5-Fluoro-2-nitroanisole
- o-Anisidine
- METHYL 2-(5-FLUORO-2-NITROPHENOXY)ACETATE
- R-(+)-OFLOXACIN
- 5-FLUORO-2-NITROPHENYL 4-(CHLOROMETHYL)BENZOATE
- 5-FLUORO-2-NITROPHENYL 3-METHYLBENZOATE
- 5-FLUORO-2-NITROPHENYL 2-FLUOROBENZOATE
- 5-FLUORO-2-NITROPHENYL 4-NITROBENZOATE
- 5-FLUORO-2-NITROPHENYL 2,6-DIFLUOROBENZOATE
- 5,5I DIFLUORO BAPTA(K+ SALT)
- 5-FLUORO-2-NITROPHENYL 2-CHLOROBENZOATE
- 5-FLUORO-2-NITROPHENYL 2-(2-METHOXYPHENYL)-5-OXOTETRAHYDROFURAN-3-CARBOXYLATE