CAS 4890-85-1
:2-(2-Phenylethyl)benzoic acid
Description:
2-(2-Phenylethyl)benzoic acid, with the CAS number 4890-85-1, is an organic compound characterized by its aromatic structure, which includes a benzoic acid moiety and a 2-phenylethyl group. This compound typically appears as a white to off-white solid and is known for its moderate solubility in organic solvents such as ethanol and acetone, while being less soluble in water. The presence of both the carboxylic acid functional group and the phenyl groups contributes to its potential applications in pharmaceuticals and organic synthesis. Its molecular structure allows for various interactions, including hydrogen bonding and π-π stacking, which can influence its reactivity and stability. Additionally, 2-(2-Phenylethyl)benzoic acid may exhibit biological activity, making it of interest in medicinal chemistry. As with many organic compounds, handling should be done with care, considering safety data and potential hazards associated with its use.
Formula:C15H14O2
InChI:InChI=1S/C15H14O2/c16-15(17)14-9-5-4-8-13(14)11-10-12-6-2-1-3-7-12/h1-9H,10-11H2,(H,16,17)
InChI key:InChIKey=IOHPVZBSOKLVMN-UHFFFAOYSA-N
SMILES:C(CC1=CC=CC=C1)C2=C(C(O)=O)C=CC=C2
Synonyms:- 2-(2-Phenethyl)benzoic acid
- 2-(2-Phenyl Ethyl) Benzoic Acid
- 2-(2-Phenylethyl)Benzoate
- 2-(2-Phenylethyl)Benzoic Acid
- 2-(Phenethyl)benzoic acid
- 2-Bibenzylcarboxylic Acid 98%
- 2-Dibenzylcarboxylic acid
- 2-Phenethylbenzoic Acid
- 2-Phenylethylbenzoic Acid
- Akos Bc-0835
- Benzoic acid, 2-(2-phenylethyl)-
- Benzoic acid, o-phenethyl-
- Labotest-Bb Lt00159422
- O-Phenethylbenzoic Acid
- See more synonyms
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Found 4 products.
2-(2-phenylethyl)benzoic acid
CAS:Formula:C15H14O2Purity:95%Color and Shape:SolidMolecular weight:226.27052-Bibenzylcarboxylic acid
CAS:Formula:C15H14O2Purity:98%+(LC-MS);RGColor and Shape:SolidMolecular weight:226.2752-Bibenzylcarboxylic acid
CAS:<p>2-Bibenzylcarboxylic acid is a synthetic retinoid that has been shown to have potent antagonistic effects against the activity of various pro-inflammatory enzymes. It blocks the integrin receptor, which prevents leukocyte adhesion and migration. 2-Bibenzylcarboxylic acid also inhibits protease activity by binding to the active site of the enzyme and preventing substrate binding, as well as dextran sulfate-induced inflammation. 2-Bibenzylcarboxylic acid has been shown to be effective in reducing disease activity in animal models of inflammatory diseases such as rheumatoid arthritis.</p>Formula:C15H14O2Purity:Min. 95%Molecular weight:226.27 g/mol



