CAS 52938-97-3
:5-phenylfuran-2-carboxylic acid
Description:
5-Phenylfuran-2-carboxylic acid is an organic compound characterized by its furan ring structure substituted with a phenyl group and a carboxylic acid functional group. The presence of the furan ring imparts aromatic properties, while the carboxylic acid group contributes to its acidity and potential for hydrogen bonding. This compound typically exhibits moderate solubility in polar solvents due to the carboxylic acid functionality, while its aromatic nature may enhance solubility in non-polar solvents. It can participate in various chemical reactions, including esterification and amidation, making it useful in organic synthesis. Additionally, the compound may exhibit biological activity, which could be of interest in pharmaceutical research. Its molecular structure allows for potential interactions with biological targets, making it a candidate for further investigation in medicinal chemistry. Overall, 5-phenylfuran-2-carboxylic acid is a versatile compound with applications in both synthetic organic chemistry and potential therapeutic contexts.
Formula:C11H8O3
InChI:InChI=1/C11H8O3/c12-11(13)10-7-6-9(14-10)8-4-2-1-3-5-8/h1-7H,(H,12,13)
SMILES:c1ccc(cc1)c1ccc(C(=O)O)o1
Synonyms:- 2-Furancarboxylic acid, 5-phenyl-
- 5-Phenyl-2-furoic acid
- IFLAB-BB F0850-6681
- 5-PHENYL-2-FURANCARBOXYLIC ACID
- TIMTEC-BB SBB009726
- 5-PHENYL-FURAN-2-CARBOXYLIC ACID
- 5-Phenylfurane-2-carboxylic acid
- 5-Phenyl-2-furoic acid 97%
- RARECHEM AL BE 0884
- ASISCHEM V38284
- 5-Phenyl-2-furancarboxylicAcid>
- ART-CHEM-BB B025035
- LABOTEST-BB LT00569128
- AKOS BAR-0049
- See more synonyms
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Found 5 products.
5-Phenyl-2-furancarboxylic Acid
CAS:Formula:C11H8O3Purity:>96.0%(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:188.185-Phenylfuran-2-carboxylic acid
CAS:Formula:C11H8O3Purity:96%Color and Shape:SolidMolecular weight:188.17945-Phenyl-2-furancarboxylic Acid
CAS:<p>5-Phenyl-2-furancarboxylic Acid is an inhibitor of methionine aminopeptidase that contains a phenyl substituent. It is non-selective and has been shown to be effective against E. coli, P. aeruginosa, and S. aureus at concentrations of less than 1 μM. The inhibition of methionine aminopeptidase by 5-phenyl-2-furancarboxylic acid results in the accumulation of methionine and other amino acids, which are substrates for peptide bond formation. This leads to the inhibition of protein synthesis through the disruption of nucleotide synthesis and cell division.</p>Formula:C11H8O3Purity:Min. 95%Molecular weight:188.18 g/mol




