(3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl)methanol is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a phenyl group and two methyl groups attached to the pyrazole ring, contributing to its unique chemical properties. The presence of a hydroxymethyl group (-CH2OH) indicates that it can participate in hydrogen bonding, enhancing its solubility in polar solvents. The molecular structure suggests potential applications in medicinal chemistry, particularly due to the pyrazole moiety, which is often associated with various biological activities. The compound's stability and reactivity can be influenced by the substituents on the pyrazole ring, making it a subject of interest for further research in drug development and synthesis. Additionally, its CAS number, 58789-53-0, allows for easy identification and reference in chemical databases. Overall, this compound exemplifies the diverse chemistry of pyrazole derivatives and their potential utility in various fields.

(3,5-dimethyl-1-phenyl-1H-pyrazol-4-yl)methanol

58789-53-0: (3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl)methanol is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a phenyl group and two methyl groups attached to the pyrazole ring, contributing to its unique chemical properties. The presence of a hydroxymethyl group (-CH2OH) indicates that it can participate in hydrogen bonding, enhancing its solubility in polar solvents. The molecular structure suggests potential applications in medicinal chemistry, particularly due to the pyrazole moiety, which is often associated with various biological activities. The compound's stability and reactivity can be influenced by the substituents on the pyrazole ring, making it a subject of interest for further research in drug development and synthesis. Additionally, its CAS number, 58789-53-0, allows for easy identification and reference in chemical databases. Overall, this compound exemplifies the diverse chemistry of pyrazole derivatives and their potential utility in various fields.

(3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl)methanol

3,5-Dimethyl-4-(hydroxymethyl)-1-phenyl-1H-pyrazole

CAS 58789-53-0

(3,5-dimethyl-1-phenyl-1H-pyrazol-4-yl)methanol

(3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl)methanol

Ref: IN-DA00EC44

3,5-Dimethyl-4-(hydroxymethyl)-1-phenyl-1H-pyrazole

Ref: 54-OR9983

(3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl)methanol

Ref: 3D-ICA78953