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:
Assay:
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%
Quality Level
functional group
carboxylic acid, fluoro
Application
2-Fluorobenzoic acid may be employed in the preparation of zaragozic acid A analogs.
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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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
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
M Begoña Osuna et al.
Water research, 42(14), 3857-3869 (2008-07-29)
Two up-flow fixed-bed reactors (UFBRs), inoculated with activated sludge and operated for 162 days, were fed 1mmolL(-1)d(-1) with two model halogenated compounds, 2-fluorobenzoate (2-FB) and dichloromethane (DCM). Expanded clay (EC) and granular activated carbon (GAC) were used as biofilm carrier.
T S Chen et al.
The Journal of antibiotics, 47(11), 1290-1294 (1994-11-01)
Zaragozic acid A analogues are produced by an unidentified sterile fungus when it is exogenously supplied with 2-thiophenecarboxylic acid, 3-thiophenecarboxylic acid, 2-furoic acid, 2-fluorobenzoic acid, 3-fluorobenzoic acid, or 4-fluorobenzoic acid. The analogues carry 2-thiophenyl, 3-thiophenyl, 2-furyl, o-fluorophenyl, m-fluorophenyl, or p-fluorophenyl
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