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Merck
CN

190276

3-Phenoxybenzoic acid

98%

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About This Item

Linear Formula:
C6H5OC6H4CO2H
CAS Number:
Molecular Weight:
214.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-121-2
Beilstein/REAXYS Number:
2105574
MDL number:
Assay:
98%
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assay

98%

mp

147-149 °C (lit.)

functional group

carboxylic acid, phenoxy

SMILES string

OC(=O)c1cccc(Oc2ccccc2)c1

InChI

1S/C13H10O3/c14-13(15)10-5-4-8-12(9-10)16-11-6-2-1-3-7-11/h1-9H,(H,14,15)

InChI key

NXTDJHZGHOFSQG-UHFFFAOYSA-N

Application

3-Phenoxybenzoic acid was used as standard in the determination of urinary residues of 3-phenoxybenzoic acid by GLC with electron-capture detection method. It was also used in the synthesis of poly(ether-ketones).


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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Articles

Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.

傅-克酰基化反应是一种芳烃与酰氯或酸酐使用强路易斯酸催化剂的反应。该反应通过亲电芳族取代进行,形成单酰化产物。


Grafting of vapor-grown carbon nanofibers via in-situ polycondensation of 3-phenoxybenzoic acid in poly (phosphoric acid).
Baek J-B, et al.
Macromolecules, 37(22), 8278-8285 (2004)
C Aprea et al.
Journal of chromatography. B, Biomedical sciences and applications, 695(2), 227-236 (1997-08-01)
The determination of urinary 3-phenoxybenzoic acid enables exposure to pyrethroid insecticides to be evaluated. A method for the quantitative determination of this metabolite in urine is described. The compound and the internal standard (2-phenoxybenzoic acid) are derivatized with pentafluorobenzylbromide and
Improved syntheses of poly (oxy-1, 3-phenylenecarbonyl-1, 4-phenylene) and related poly (ether-ketones) using polyphosphoric acid/P 2 O 5 as polymerization medium.
Baek J-B and Tan L-S.
Polymer, 44(15), 4135-4147 (2003)



Global Trade Item Number

SKUGTIN
190276-25G04061831828764
190276-5G04061838759726