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418846

Sigma-Aldrich

4-Fluorobenzoic acid

99%, purified by sublimation

Sinónimos:

p-Fluorobenzoic acid

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About This Item

Fórmula lineal:
FC6H4CO2H
Número de CAS:
456-22-4
Peso molecular:
140.11
Beilstein/REAXYS Number:
1906922
EC Number:
207-259-0
MDL number:
MFCD00002530
UNSPSC Code:
12352100
PubChem Substance ID:
24866245
NACRES:
NA.22

Quality Level

100

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

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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2,4,6-Trichlorophenol 98%

Sigma-Aldrich

T55301

2,4,6-Trichlorophenol

4-Chlorobenzoic acid 99%

Sigma-Aldrich

135585

4-Chlorobenzoic acid

4-Iodobenzoic acid 98%

Sigma-Aldrich

206547

4-Iodobenzoic acid

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)
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
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
Julien Andriès et al.
Bioorganic & medicinal chemistry letters, 20(12), 3730-3733 (2010-05-18)
In search of a serotonin 5-HT(7) radiotracer for positron emission tomography, we developed 1-[2-[(2S)-1-(phenylsulfonyl)pyrrolidin-2-yl]ethyl]piperidin-4-yl 4-fluorobenzoate. After labeling in good yield with fluorine-18 via nitro for fluorine exchange, preliminary biological experiments with autoradiographies failed to evidence any specific 5-HT(7) receptor delineation.
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)
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