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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:
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.
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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Victor L Rendina et al.
The Journal of organic chemistry, 77(2), 1181-1185 (2012-01-14)
A new protocol for titrating nonstabilized diazoalkane solutions by quantitative (19)F NMR is reported. An excess of 2-fluorobenzoic acid dissolved in CDCl(3) is treated with the diazoalkane solution at a low temperature, immediately forming the corresponding 2-fluorobenzoate ester upon warming.
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
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
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.
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
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