CAS 772-15-6
:(+)-3-Phenylbutyric acid
Description:
(+)-3-Phenylbutyric acid, with the CAS number 772-15-6, is an organic compound characterized by its phenyl group attached to a butyric acid backbone. This compound is a chiral molecule, meaning it exists in two enantiomeric forms, with the (+) designation indicating the specific optical activity of this isomer. It typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. The compound is known for its role in various biochemical applications, including its potential use in pharmaceuticals and as a building block in organic synthesis. Its structure features a carboxylic acid functional group, which contributes to its acidity and reactivity. Additionally, (+)-3-Phenylbutyric acid has been studied for its effects on cellular processes and its potential therapeutic applications, particularly in the context of neuroprotection and metabolic disorders. As with many organic acids, it is soluble in organic solvents and exhibits limited solubility in water. Proper handling and storage are essential due to its chemical properties.
Formula:C10H12O2
InChI:InChI=1S/C10H12O2/c1-8(7-10(11)12)9-5-3-2-4-6-9/h2-6,8H,7H2,1H3,(H,11,12)/t8-/m0/s1
InChI key:InChIKey=ZZEWMYILWXCRHZ-QMMMGPOBSA-N
SMILES:[C@@H](CC(O)=O)(C)C1=CC=CC=C1
Synonyms:- (βS)-β-Methylbenzenepropanoic acid
- Benzenepropanoic acid, β-methyl-, (S)-
- Hydrocinnamic acid, β-methyl-, (S)-
- Benzenepropanoic acid, β-methyl-, (βS)-
- (S)-(+)-β-Methylhydrocinnamic acid
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Found 3 products.
(S)-3-Phenylbutyric acid
CAS:Formula:C10H12O2Purity:97%Color and Shape:LiquidMolecular weight:164.2011(S)-3-Phenylbutyric Acid
CAS:<p>(S)-3-Phenylbutyric Acid is a chiral compound that has been synthesized using the asymmetric synthesis method. The conformational properties of this compound have been studied in detail and its optical activity has been determined. Its hydrolysis products are cinnamic acid and phenylacetic acid, which can be analyzed through spectrometry. It is used as an analytical tool for determining the enantiomeric purity of butyric acid, as well as being used for optimization purposes. (S)-3-Phenylbutyric Acid also shows high uptake in bacteria, yeast, and mammalian cells, which may be due to its magnetic resonance properties.</p>Formula:C10H12O2Purity:Min. 95%Molecular weight:164.2 g/mol


