CAS 90005-62-2
:α-Methyl-3-pyridineacetic acid
Description:
α-Methyl-3-pyridineacetic acid, with the CAS number 90005-62-2, is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a methyl group and an acetic acid moiety attached to the pyridine ring, contributing to its unique chemical properties. It is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the carboxylic acid functional group. The compound exhibits acidic behavior due to the carboxylic acid group, which can donate protons in solution. Its structural features may impart biological activity, making it of interest in pharmaceutical research. Additionally, α-Methyl-3-pyridineacetic acid can participate in various chemical reactions, including esterification and amidation, which are relevant in synthetic organic chemistry. Overall, this compound's characteristics make it a valuable substance in both academic and industrial applications.
Formula:C8H9NO2
InChI:InChI=1S/C8H9NO2/c1-6(8(10)11)7-3-2-4-9-5-7/h2-6H,1H3,(H,10,11)
InChI key:InChIKey=RVSGAPGURIPIFA-UHFFFAOYSA-N
SMILES:C(C(O)=O)(C)C=1C=CC=NC1
Synonyms:- α-Methylpyridine-3-acetic acid
- 2-(Pyridin-3-yl)propanoic acid
- 3-Pyridineacetic acid, α-methyl-
- 2-Pyridin-3-yl-propionic acid
- α-Methyl-3-pyridineacetic acid
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Found 3 products.
2-(Pyridin-3-yl)propanoic acid
CAS:2-(Pyridin-3-yl)propanoic acidPurity:95%Molecular weight:151.16g/mol2-(Pyridin-3-yl)propanoic acid
CAS:<p>2-(Pyridin-3-yl)propanoic acid is a quinoline derivative that has been shown to be safe and effective in clinical trials. It is being tested for the treatment of type 2 diabetes, obesity, and metabolic syndrome. The oral administration of this drug inhibits the activity of dipeptidyl peptidase-4 (DPP-4), which is an enzyme involved in the degradation of insulin. This inhibition leads to increased levels of insulin in the blood and improved glucose tolerance. 2-(Pyridin-3-yl)propanoic acid interacts with other drugs through competitive inhibition at their binding sites on enzymes. Optimization experiments have shown that it can interact with pyridine compounds, which are found in many drugs including acetaminophen and caffeine.</p>Formula:C8H9NO2Purity:Min. 95%Molecular weight:151.16 g/mol


