412244
2-Fluorbenzoesäure
97%
Synonym(e):
o-Fluorobenzoic acid
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(3)
About This Item
Lineare Formel:
FC6H4CO2H
CAS-Nummer:
Molekulargewicht:
140.11
Beilstein:
971265
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
97%
mp (Schmelzpunkt)
122-125 °C (lit.)
SMILES String
OC(=O)c1ccccc1F
InChI
1S/C7H5FO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)
InChIKey
NSTREUWFTAOOKS-UHFFFAOYSA-N
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Anwendung
2-Fluorobenzoic acid may be employed in the preparation of zaragozic acid A analogs.
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Persönliche Schutzausrüstung
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.
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.
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
Microbial degradation of synthetic organochlorine compounds.
K Motosugi et al.
Experientia, 39(11), 1214-1220 (1983-11-15)
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