418846
4-Fluorobenzoic acid
99%, purified by sublimation
Synonym(s):
p-Fluorobenzoic acid
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About This Item
Linear Formula:
FC6H4CO2H
CAS Number:
Molecular Weight:
140.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-259-0
Beilstein/REAXYS Number:
1906922
MDL number:
Product Name
4-Fluorobenzoic acid, 99%, purified by sublimation
InChI key
BBYDXOIZLAWGSL-UHFFFAOYSA-N
InChI
1S/C7H5FO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)
SMILES string
OC(=O)c1ccc(F)cc1
assay
99%
purified by
sublimation
mp
182-184 °C (lit.)
functional group
carboxylic acid
fluoro
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
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
Jan Marik et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 65(2), 199-203 (2006-08-29)
The widely used bifunctional labeling reagent 4-[18F]fluorobenzoic acid ([18F]FBA) and its activated form N-succinimidyl 4-[18F]fluorobenzoate ([18F]SFB) were prepared using a modified Siemens/CTI chemistry process control unit (CPCU) double vessel [18F]FDG module. The products were obtained with a radiochemical yield greater
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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