CAS 32852-81-6
:3-Phenoxyphenylacetic acid
Description:
3-Phenoxyphenylacetic acid is an organic compound characterized by its phenoxy and phenylacetic acid functional groups. It typically appears as a white to off-white solid and is soluble in organic solvents, while exhibiting limited solubility in water. The compound features a phenoxy group, which contributes to its aromatic properties, and an acetic acid moiety that imparts acidic characteristics. Its molecular structure allows for potential applications in pharmaceuticals and agrochemicals, particularly as a building block in the synthesis of various biologically active compounds. The compound may exhibit biological activity, including potential anti-inflammatory or analgesic effects, although specific biological properties can vary based on structural modifications and the presence of substituents. As with many organic acids, it is important to handle 3-Phenoxyphenylacetic acid with care, following appropriate safety protocols to mitigate any risks associated with its use.
Formula:C14H12O3
InChI:InChI=1/C14H12O3/c15-14(16)10-11-5-4-8-13(9-11)17-12-6-2-1-3-7-12/h1-9H,10H2,(H,15,16)
SMILES:c1ccc(cc1)Oc1cccc(c1)CC(=O)O
Synonyms:- 3-Phenoxyphenylacetic
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Found 6 products.
3-Phenoxyphenylacetic acid, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C14H12O3Purity:98%Molecular weight:228.252-(3-phenoxyphenyl)acetic acid
CAS:Formula:C14H12O3Purity:96%Color and Shape:SolidMolecular weight:228.24333-Phenoxyphenylacetic acid
CAS:<p>3-Phenoxyphenylacetic acid is a diphenyl ether compound. It is used as a preservative and has antimycobacterial activity. 3-Phenoxyphenylacetic acid has been shown to be active against tuberculosis, with an MIC of 0.5 ug/mL. In addition, it can inhibit the growth of methicillin-resistant Staphylococcus aureus (MRSA) and erythromycin-resistant Mycobacterium tuberculosis. The mechanism of action is not fully understood, but may involve the inhibition of electron transport or oxidative phosphorylation in bacterial cells. 3-Phenoxyphenylacetic acid also inhibits the formation of reactive oxygen species from NADPH oxidase in human neutrophils, which may contribute to its antimicrobial activity.</p>Formula:C14H12O3Purity:Min. 95%Color and Shape:PowderMolecular weight:228.24 g/mol3-Phenoxyphenylacetic acid
CAS:Formula:C14H12O3Purity:96%Color and Shape:Solid, No data available.Molecular weight:228.247





