3-(4-Methylpiperazin-1-yl)phenylmethanol, identified by its CAS number 123987-13-3, is an organic compound characterized by the presence of a phenyl group attached to a methanol moiety, with a 4-methylpiperazine substituent. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the hydroxyl group in the methanol part of its structure. The piperazine ring contributes to its potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the methyl group on the piperazine enhances its lipophilicity, which can influence its pharmacokinetic properties. Additionally, the compound may engage in hydrogen bonding due to the hydroxyl group, affecting its interactions with biological targets. Overall, 3-(4-methylpiperazin-1-yl)phenylmethanol is a compound with notable structural features that may confer specific chemical reactivity and biological activity.

3-(4-METHYLPIPERAZIN-1-YL)PHENYL]METHANOL

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(3-(4-Methylpiperazin-1-yl)phenyl)methanol

Benzenemethanol, 3-(4-methyl-1-piperazinyl)-

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CAS 123987-13-3: 3-(4-METHYLPIPERAZIN-1-YL)PHENYL]METHANOL

(3-(4-Methylpiperazin-1-yl)phenyl)methanol

Ref: 10-F077520

Benzenemethanol, 3-(4-methyl-1-piperazinyl)-

Ref: IN-DA000LB7

[3-(4-Methylpiperazin-1-yl)phenyl]methanol

Ref: 3D-FM35772

(3-(4-Methylpiperazin-1-yl)phenyl)methanol

Ref: 54-OR301206