(R)-4-Benzyl-2-hydroxymethylpiperazine

98%

Reagent Code: #231127
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CAS Number 149715-46-8

science Other reagents with same CAS 149715-46-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.28 g/mol
Formula C₁₂H₁₈N₂O
badge Registry Numbers
MDL Number MFCD11113046
thermostat Physical Properties
Boiling Point 318.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.083 g/cm3
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its piperazine core with a hydroxymethyl and benzyl group enables selective interactions in drug design, enhancing bioavailability and target specificity. Commonly employed in the preparation of bioactive molecules requiring stereochemical control, such as serotonin or dopamine receptor ligands. Also utilized in the creation of protease inhibitors and antimicrobial compounds due to its ability to mimic peptide motifs and improve metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,090.00

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(R)-4-Benzyl-2-hydroxymethylpiperazine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its piperazine core with a hydroxymethyl and benzyl group enables selective interactions in drug design, enhancing bioavailability and target specificity. Commonly employed in the preparation of bioactive molecules requiring stereochemical control, such as serotonin or dopamine receptor ligands. Also utilized in the creation of protease inhibitors

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its piperazine core with a hydroxymethyl and benzyl group enables selective interactions in drug design, enhancing bioavailability and target specificity. Commonly employed in the preparation of bioactive molecules requiring stereochemical control, such as serotonin or dopamine receptor ligands. Also utilized in the creation of protease inhibitors and antimicrobial compounds due to its ability to mimic peptide motifs and improve metabolic stability.

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