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Methyl 4-amino-2-fluorobenzoate

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Methyl 4-amino-2-fluorobenzoate manufacturers

Methyl 4-amino-2-fluorobenzoate Basic information
Product Name:Methyl 4-amino-2-fluorobenzoate
Synonyms:2-Fluoro-4-aminobenzoic acid methyl ester;Methyl 2-fluoro-4-aminobenzoate;Benzoic acid,4-aMino-2-fluoro-, Methyl ester;EnzalutamideImpurity45;Benzoic acid, 4-amino-2-fluoro-, methyl ester (9CI, ACI);4-amino-2-fluoro-Benzoic acid methyl ester (9CI ACI);Methyl 4-helium-2-fluorobenzoate;Methyl 4-amino-2-fluorobenzoate
CAS:73792-08-2
MF:C8H8FNO2
MW:169.15
EINECS:
Product Categories:
Mol File:73792-08-2.mol
Methyl 4-amino-2-fluorobenzoate Structure
Methyl 4-amino-2-fluorobenzoate Chemical Properties
Melting point Too Dark to Visualize
Boiling point 302.3±27.0 °C(Predicted)
density 1.264±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka1.45±0.10(Predicted)
form Solid
color Orange to Brown
Safety Information
HS Code 2916399090
MSDS Information
Methyl 4-amino-2-fluorobenzoate Usage And Synthesis
UsesMethyl 4-amino-2-fluorobenzoate is mainly used as an intermediate in organic synthesis, especially in the field of pharmaceutical manufacturing.
Synthesis
METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE

392-09-6

METHYL 4-AMINO-2-FLUOROBENZOATE

73792-08-2

Step 2: Methyl 2-fluoro-4-nitrobenzoate (1.05 g, 5.273 mmol) was dissolved in methanol (MeOH). Palladium/carbon (Pd/C, 105 mg) was added to the resulting solution. The reaction mixture was stirred for 2 hours at room temperature in a hydrogen (H2) atmosphere. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad to remove the catalyst. The filtrate was concentrated under reduced pressure to give the crude product. The crude product was purified by column chromatography to give the final pure methyl 4-amino-2-fluorobenzoate (870 mg, 98% yield).

References[1] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 19, p. 7042 - 7051
[2] Patent: WO2013/68467, 2013, A1. Location in patent: Page/Page column 57; 59; 60; 61
[3] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 2, p. 337 - 343
[4] Patent: WO2004/14900, 2004, A1. Location in patent: Page 52
[5] Journal of Organic Chemistry, 1990, vol. 55, # 7, p. 2034 - 2044
Methyl 4-amino-2-fluorobenzoate Preparation Products And Raw materials
Raw materialsMethyl 2-fluoro-4-nitrobenzenecarboxylate-->Methanol-->4-Amino-2-fluorobenzoic acid-->Palladium-->Hydrogen-->Activated carbon
Preparation Productsmethyl 4-(chlorosulfonyl)-2-fluorobenzoate
Tag:Methyl 4-amino-2-fluorobenzoate(73792-08-2) Related Product Information
Enzalutamide Impurity 7 4-Amino-2-fluoro-N,N-dimethylbenzamide Benzamide, 4-amino-2-fluoro- (9CI) Benzamide, 4-[3-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-5,5-dimethyl-4-oxo-1-imidazolidinyl]-2-fluoro-N-methyl- Enzalutamide Impurity 1 4-isothiocyanato-2-(trifluoroMethyl)benzonitrile 4-Amino-2-(trifluoromethyl)benzamide 2-Fluoro-4-nitrobenzoic acid Benzoic acid, 4-isothiocyanato-2-(trifluoromethyl)- Enzalutamide Impurity 7 4-[1-(4-cyano-3-trifluoromethyl-phenylcarbamoyl)-1-methyl-ethylamino]-2-fluoro-N- 4-amino-2-fluoro-N-methylbenzamide 4-Bromo-2-fluoro-N-methylbenzamide 4-Amino-2-fluorobenzoic acid 4-Nitro-2-(trifluoromethyl)benzonitrile 2-Fluoro-N-methyl-4-nitrobenzamide 4-Amino-2-trifluoromethylbenzoic acid 4-Bromo-2-fluorobenzamide