(2R,5R)-rel-2,5-Dimethylpiperazine

≥98%

Reagent Code: #232221
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CAS Number 6284-84-0

science Other reagents with same CAS 6284-84-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 114.19 g/mol
Formula C₆H₁₄N₂
badge Registry Numbers
MDL Number MFCD00137758
thermostat Physical Properties
Melting Point 114 °C
Boiling Point 165.9 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its rigid piperazine backbone with defined stereocenters makes it valuable in medicinal chemistry for designing drugs with improved selectivity and metabolic stability. Commonly employed in the preparation of kinase inhibitors, antimicrobial agents, and central nervous system (CNS) active compounds. Also utilized in asymmetric synthesis and catalysis as a ligand or auxiliary due to its ability to induce stereoselectivity in chemical reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿72,300.00
(2R,5R)-rel-2,5-Dimethylpiperazine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its rigid piperazine backbone with defined stereocenters makes it valuable in medicinal chemistry for designing drugs with improved selectivity and metabolic stability. Commonly employed in the preparation of kinase inhibitors, antimicrobial agents, and central nervous system (CNS) active compou

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its rigid piperazine backbone with defined stereocenters makes it valuable in medicinal chemistry for designing drugs with improved selectivity and metabolic stability. Commonly employed in the preparation of kinase inhibitors, antimicrobial agents, and central nervous system (CNS) active compounds. Also utilized in asymmetric synthesis and catalysis as a ligand or auxiliary due to its ability to induce stereoselectivity in chemical reactions.

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