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Merck

412244

2-Fluorobenzoic acid

97%

Sinónimos:

o-Fluorobenzoic acid

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25 G

MXP 943.00

100 G

MXP 1,892.00

MXP 943.00


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Fórmula lineal:
FC6H4CO2H
Número CAS:
Peso molecular:
140.11
Beilstein/REAXYS Number:
971265
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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assay

97%

mp

122-125 °C (lit.)

functional group

carboxylic acid
fluoro

SMILES string

OC(=O)c1ccccc1F

InChI

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

InChI key

NSTREUWFTAOOKS-UHFFFAOYSA-N

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Este artículo
F6605703931535982
assay

97%

assay

97%

assay

97%

assay

97%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

122-125 °C (lit.)

mp

122-124 °C (lit.)

mp

215-219 °C

mp

152-157 °C (lit.)

functional group

carboxylic acid

functional group

-

functional group

carboxylic acid, fluoro, nitrile

functional group

carboxylic acid, chloro, fluoro

Application

2-Fluorobenzoic acid may be employed in the preparation of zaragozic acid A analogs.[1]

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Clase de almacenamiento

11 - Combustible Solids

wgk_germany

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.
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.
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
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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