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Names | |||
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Preferred IUPAC name 4-Fluorobenzoic acid | |||
Other names p-fluorobenzoic acid, para-fluorobenzoic acid, 4-fluoro-benzoic acid | |||
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ECHA InfoCard | 100.006.600 | ||
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Properties | |||
Chemical formula | C7H5FO2 | ||
Molar mass | 140.113 g·mol | ||
Appearance | white solid | ||
Density | 1.479 g/cm | ||
Melting point | 184 °C (363 °F; 457 K) | ||
Boiling point | 253.687 °C (488.637 °F; 526.837 K) at 760 mmHg | ||
Solubility in water | 1200 mg/L | ||
log P | 2.07 | ||
Acidity (pKa) | 4.14 | ||
Hazards | |||
Occupational safety and health (OHS/OSH): | |||
Main hazards | Irritates lungs, eyes, skin | ||
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Signal word | Danger | ||
Hazard statements | H302, H318 | ||
Precautionary statements | P264, P270, P280, P301+P312, P305+P351+P338, P310, P330, P501 | ||
Flash point | 107.226 °C (225.007 °F; 380.376 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
4-Fluorobenzoic acid (p-fluorobenzoic acid) is an organic compound with the formula C7H5FO2. This colourless solid is a derivative of benzoic acid carboxylic acid. It is a synthetic intermediate.
Preparation
4-Fluorobenzoic acid is commercially available. It may be prepared via the Schiemann reaction, in which a 4-aminobenzoic acid, protected as the ethyl ester, is diazotised and then fluoride introduced using tetrafluoroborate. Hydrolysis of the ester converts it back to the free acid.
4-Fluorobenzoic acid has been observed to form by the aerobic biotransformation of 4-fluorocinnamic acid.
See also
References
- GHS: PubChem 9973
- G. Schiemann; W. Winkelmüller (1943). "p-Fluorobenzoic Acid". Organic Syntheses; Collected Volumes, vol. 2, p. 299.
- Freitas Dos Santos, Luisa M.; Spicq, Arnaud; New, Anthony P.; Lo Biundo, Giuseppe; Wolff, Jean-Claude; Edwards, Andrew (2001). "Aerobic biotransformation of 4-fluorocinnamic acid to 4-fluorobenzoic acid". Biodegradation. 12 (1): 23–9. doi:10.1023/A:1011973824171. PMID 11693292. S2CID 30830147.