(S)-4-benzyl-2-hydroxymethylpiperazine is a chiral organic compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. The presence of a benzyl group at the 4-position and a hydroxymethyl group at the 2-position contributes to its unique chemical properties. This compound is typically a white to off-white solid and is soluble in polar solvents, reflecting its functional groups' ability to engage in hydrogen bonding. The hydroxymethyl group enhances its reactivity, making it a potential candidate for further chemical modifications or applications in medicinal chemistry. As a chiral molecule, it may exhibit different biological activities depending on its stereochemistry, which is crucial in drug development. Its CAS number, 149715-45-7, allows for easy identification in chemical databases and literature. Overall, (S)-4-benzyl-2-hydroxymethylpiperazine is of interest in various fields, including pharmaceuticals and organic synthesis, due to its structural features and potential biological implications.

(S)-4-benzyl-2-hydroxymethylpiperazine

149715-45-7: [(2S)-4-Benzylpiperazin-2-yl]methanol, 2-piperazinemethanol, 4-(phenylmethyl)-, (2S)-, (S)-4-Benzyl-2-Hydroxymethylpiperazine 2Hcl

CAS 149715-45-7: (S)-4-benzyl-2-hydroxymethylpiperazine

(S)-4-Benzyl-2-hydroxymethylpiperazine

Ref: 54-OR451102

2-Piperazinemethanol, 4-(phenylmethyl)-, (2S)-

Ref: IN-DA001LYD

(S)-4-Benzyl-2-Hydroxymethylpiperazine

Ref: 10-F235111

(S)-4-Benzyl-2-hydroxymethylpiperazine

Ref: 3D-ZFA71545