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Merck
CN

412244

2-Fluorobenzoic acid

97%

Synonym(s):

o-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:
207-158-1
Beilstein/REAXYS Number:
971265
MDL number:
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Product Name

2-Fluorobenzoic acid, 97%

InChI key

NSTREUWFTAOOKS-UHFFFAOYSA-N

InChI

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

SMILES string

OC(=O)c1ccccc1F

assay

97%

mp

122-125 °C (lit.)

functional group

carboxylic acid
fluoro

Quality Level

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Application

2-Fluorobenzoic acid may be employed in the preparation of zaragozic acid A analogs.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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U Schennen et al.
Journal of bacteriology, 161(1), 321-325 (1985-01-01)
Three strains of anaerobically benzoate-degrading, denitrifying bacteria of the genus Pseudomonas were able to grow on 2-fluorobenzoate as the sole carbon and energy source. Fluoride ion release was stoichiometric, and the reduction of dissolved organic carbon indicated total degradation. Cells
Microbial degradation of synthetic organochlorine compounds.
K Motosugi et al.
Experientia, 39(11), 1214-1220 (1983-11-15)
J Toretsky et al.
Nuclear medicine and biology, 31(6), 747-752 (2004-07-13)
The clinical response to antitumor therapy is measured using imaging, such as CT or MRI, 6-12 weeks following chemotherapy treatment. The images at that time reflect both tumor cell death and new growth. Therefore, the amount of tumor cell death
S Y Lee et al.
Nuclear medicine and biology, 28(4), 391-395 (2001-06-08)
In vitro metabolism of acetylcholinesterase inhibitors containing 3-[(18)F]fluoromethylbenzyl- ([(18)F]1) and 4-[(18)F]fluorobenzyl-piperidine moieties ([(18)F]2) was studied and compared with the in vivo metabolism. Defluorination of the [(18)F]1 mainly occurred to generate [(18)F]fluoride ion both in vitro and in vivo. In contrast
O Drzyzga et al.
FEMS microbiology letters, 116(2), 215-219 (1994-02-15)
A mesophilic, dehalogenating, sulfate-reducing diculture was isolated from an anaerobic lake sediment. One strain of the diculture is proposed to be an endospore-forming Desulfotomaculum species, the second strain was a vibrioid, motile and non-sporeforming species which is tentatively assigned to

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