CAS 82231-51-4

4-methyl-1H-pyrazole-5-carboxylic acid

Description:

4-Methyl-1H-pyrazole-5-carboxylic acid is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a carboxylic acid functional group (-COOH) at the 5-position and a methyl group (-CH3) at the 4-position of the pyrazole ring. It is typically a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the carboxylic acid group. The compound is of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential biological activities and applications. Its reactivity can be attributed to the acidic nature of the carboxylic group and the electron-rich nitrogen atoms in the pyrazole ring, which can participate in various chemical reactions. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₅H₆N₂O₂

InChI: InChI=1/C5H6N2O2/c1-3-2-6-7-4(3)5(8)9/h2H,1H3,(H,6,7)(H,8,9)

SMILES: Cc1c[nH]nc1C(=O)O

Synonyms:

• 1H-Pyrazole-3-carboxylic acid, 4-methyl-
• 4-Methyl-1H-pyrazole-3-carboxylic acid
• 4-Methylpyrazole-5-carboxylic acid
• 82231-51-4

4-methyl-1H-pyrazole-3-carboxylic acid

CAS: 82231-51-4

Formula: C₅H₆N₂O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 126.1133

Ref: IN-DA003LSK

4-Methylpyrazole-3-carboxylic acid

CAS: 82231-51-4

4-Methylpyrazole-3-carboxylic acid

Purity: 98%

Molecular weight: 126.11g/mol

Ref: 54-OR951257

4-Methyl-1H-pyrazole-3-carboxylic acid

CAS: 82231-51-4

Formula: C₅H₆N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 126.115

Ref: 10-F447043

4-Methylpyrazole-3-carboxylic acid

CAS: 82231-51-4

4-Methylpyrazole-3-carboxylic acid is a monocarboxylic acid. It is a byproduct of the reaction between chloride and hydrogen chloride. 4-Methylpyrazole-3-carboxylic acid has been shown to have carcinogenic properties in animals, but not in humans. The mechanism for this effect is thought to be due to its ability to inhibit IL-17a production, which may lead to an increase in tumor growth. 4-Methylpyrazole-3-carboxylic acid has been shown to inhibit muscle glycogen synthesis and focus formation. It also inhibits the oxidation of fatty acids by binding with the enzyme acyl CoA oxidase. This compound can be used as an agrochemical and dechlorinated organic solvent for the extraction of phenylephrine from plants like tobacco leaves.

Formula: C₅H₆N₂O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 126.11 g/mol

Ref: 3D-HDA23151