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418846

Sigma-Aldrich

4-Fluorobenzoic acid

99%, purified by sublimation

Synonym(s):

p-Fluorobenzoic acid

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About This Item

Linear Formula:
FC6H4CO2H
CAS Number:
456-22-4
Molecular Weight:
140.11
Beilstein:
1906922
EC Number:
207-259-0
MDL number:
MFCD00002530
UNSPSC Code:
12352100
PubChem Substance ID:
24866245
NACRES:
NA.22

Assay

99%

purified by

sublimation

mp

182-184 °C (lit.)

SMILES string

OC(=O)c1ccc(F)cc1

InChI

1S/C7H5FO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)

InChI key

BBYDXOIZLAWGSL-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Biodegradation studies of 4-fluorobenzoic acid and 4-fluorocinnamic acid: an evaluation of membrane inlet mass spectrometry as an alternative to high performance liquid chromatography and ion chromatography.
Creaser C, et al.
Analytica Chimica Acta, 454(1), 137-145 (2002)
Preparation of 4-fluorophenol and 4-fluorobenzoic acid by the Baeyer-Villiger reaction.
Conte L, et al.
Journal of Fluorine Chemistry, 67(1), 41-45 (1994)
Benjamin J Hackel et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 54(7), 1101-1105 (2013-05-15)
Integrin αvβ6 is a cell surface receptor minimally expressed by healthy tissue but elevated in lung, colon, skin, ovarian, cervical, and pancreatic cancers. A molecular PET agent for integrin αvβ6 could provide significant clinical utility by facilitating both cancer staging
Richard E Carson et al.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 23(2), 249-260 (2003-02-07)
The 5-HT1A ligands [ 18F]FPWAY and [ 18F]FCWAY are metabolized to [ 18F]fluorobenzoic acid (FB) and [ 18F]fluorocyclohexanecarboxylic acid (FC), respectively. To quantify the penetration of these acids into the brain, dynamic positron emission tomography studies were performed in rhesus
J L Sutcliffe-Goulden et al.
Bioorganic & medicinal chemistry letters, 10(14), 1501-1503 (2000-07-29)
A strategy for the solid phase synthesis of [18F]labelled peptides has been developed. The peptides were prepared on solid support and acylated with 4-[18F]fluorobenzoic acid using HATU within 3 min and the labelled peptide was released from the solid support
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