2-Fluoro-4-methoxybenzoic acid
2-Fluoro-4-methoxybenzoic acid Basic information
- Product Name:
- 2-Fluoro-4-methoxybenzoic acid
- Synonyms:
-
- 2-FLUORO-P-ANISIC ACID
- BUTTPARK 32\01-80
- RARECHEM AL BE 0456
- 4-Carboxy-3-fluoroanisole, 2-Fluoro-p-anisic acid
- 2-Fluoro-4-methoxybenzoicAcid>
- Benzoic acid, 2-fluoro-4-methoxy-
- 2-FLUORO-4-METHOXYBENZOIC ACID
- 2-Fluoro-4-methoxybenzoic acid 98%
- CAS:
- 394-42-3
- MF:
- C8H7FO3
- MW:
- 170.14
- EINECS:
- 237-589-0
- Product Categories:
-
- FINE Chemical & INTERMEDIATES
- Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
- Benzoic acid
- Mol File:
- 394-42-3.mol
2-Fluoro-4-methoxybenzoic acid Chemical Properties
- Melting point:
- 194-198°C
- Boiling point:
- 257.8±20.0 °C(Predicted)
- Density
- 1.307±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 3.54±0.10(Predicted)
- color
- White to Light yellow to Light orange
- InChI
- InChI=1S/C8H7FO3/c1-12-5-2-3-6(8(10)11)7(9)4-5/h2-4H,1H3,(H,10,11)
- InChIKey
- UPWMPIKNUXTWFP-UHFFFAOYSA-N
- SMILES
- C(O)(=O)C1=CC=C(OC)C=C1F
- CAS DataBase Reference
- 394-42-3(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36/37/38-22
- Safety Statements
- 26-36-37
- HazardClass
- IRRITANT
- HS Code
- 29163990
2-Fluoro-4-methoxybenzoic acid Usage And Synthesis
Chemical Properties
White solid
Antimicrobial activity
2-Fluoro-4-methoxybenzoic acid (2FMBA) is a potent antimicrobial agent that inhibits the growth of bacteria, fungi and other microorganisms. 2FMBA has significant antibacterial activity against Gram-positive and Gram-negative bacteria and also has significant antifungal activity against Candida albicans. 2FMBA is active in the presence of light and is a strong acid. It can be synthesized by refluxing benzoic acid with hydrazine, or by reacting an aromatic carboxylic acid with oxychloride. 2FMBA is used to treat bacterial infections such as E. coli, Staphylococcus, Salmonella, Shigella and Mycoplasma; fungal infections such as Candida albicans; and protozoal infections such as Giardia lamblia.
Synthesis
331-64-6
394-42-3
Step a) 2-fluoro-4-methoxybenzaldehyde (15 g, 97.4 mmol) was added to a mixture of silver oxide (Ag2O, 13.5 g, 58.4 mmol), sodium hydroxide (NaOH, 19.5 g, 487 mmol), and water (200 mL) preheated to 55 °C. The reaction mixture was stirred at 55 °C for 1 h. Subsequently, it was filtered and the precipitated solid was washed with hot water (10 mL). The filtrate was slowly added to 5N hydrochloric acid (HCl) pre-cooled to 0°C under vigorous stirring. The precipitated solid was filtered, washed with water and dried to give 2-fluoro-4-methoxybenzoic acid as a white solid (13.6 g, 82% yield, melting point 194-196°C); mass spectrum (MS) showed m/e 169 (M-H)+.
References
[1] Patent: US2003/199562, 2003, A1
[2] Patent: US2006/46968, 2006, A1. Location in patent: Page/Page column 28-29
[3] Journal of the Chemical Society, 1929, p. 1639
[4] RSC Advances, 2016, vol. 6, # 38, p. 32319 - 32327
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