3-Methyl-1-(4-methylphenyl)-1H-pyrazole-5-carboxylic acid, with the CAS number 885-46-1, 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, contributing to its acidic properties. The presence of a methyl group at the 3-position and a para-methylphenyl group at the 1-position enhances its hydrophobic characteristics, influencing its solubility and reactivity. Typically, compounds of this nature exhibit biological activity, making them of interest in pharmaceutical research. The carboxylic acid group can participate in hydrogen bonding, affecting its interactions in biological systems. Additionally, the compound's molecular structure suggests potential applications in agrochemicals or as intermediates in organic synthesis. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in both laboratory and industrial settings. Overall, this compound exemplifies the diverse chemistry associated with substituted pyrazoles.

3-methyl-1-(4-methylphenyl)-1H-pyrazole-5-carboxylic acid

885-46-1: 3-Methyl-1-(4-methylphenyl)-1H-pyrazole-5-carboxylic acid, with the CAS number 885-46-1, 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, contributing to its acidic properties. The presence of a methyl group at the 3-position and a para-methylphenyl group at the 1-position enhances its hydrophobic characteristics, influencing its solubility and reactivity. Typically, compounds of this nature exhibit biological activity, making them of interest in pharmaceutical research. The carboxylic acid group can participate in hydrogen bonding, affecting its interactions in biological systems. Additionally, the compound's molecular structure suggests potential applications in agrochemicals or as intermediates in organic synthesis. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in both laboratory and industrial settings. Overall, this compound exemplifies the diverse chemistry associated with substituted pyrazoles.

CAS 885-46-1

3-methyl-1-(4-methylphenyl)-1H-pyrazole-5-carboxylic acid

3-Methyl-1-p-tolyl-1h-pyrazole-5-carboxylic acid

Ref: IN-DA00GVRI

3-Methyl-1-p-tolyl-1H-pyrazole-5-carboxylic acid

Ref: 10-F023802