(2R,5R)-tert-Butyl 2,5-dimethylpiperazine-1-carboxylate

≥95%

Reagent Code: #70873
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CAS Number 1240586-48-4

science Other reagents with same CAS 1240586-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.30 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD08686669
thermostat Physical Properties
Boiling Point 280°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This chiral compound, specifically the (2R,5R)-enantiomer of tert-butyl 2,5-dimethylpiperazine-1-carboxylate, serves as a key building block and intermediate in pharmaceutical and chemical synthesis. The Boc protecting group on the piperazine ring enables selective functionalization and is valuable for constructing enantiomerically pure piperazine-containing molecules, which are common scaffolds in active pharmaceutical ingredients (APIs) for drugs targeting various biological pathways. Its defined stereochemistry ensures precise control essential for drug efficacy and safety. The compound's stability and reactivity support its use in multi-step organic syntheses aimed at developing novel therapeutics.

format_list_bulleted Product Specification

Test Parameter Specification
APPEARANCE Colorless to light yellow to -yellow Liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure
Specific Rotation [a]20/D(c=1 in EtOH) -50--44

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,469.00
inventory 100mg
10-20 days ฿3,996.00
inventory 250mg
10-20 days ฿6,984.00
inventory 5g
10-20 days ฿58,689.00

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(2R,5R)-tert-Butyl 2,5-dimethylpiperazine-1-carboxylate
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This chiral compound, specifically the (2R,5R)-enantiomer of tert-butyl 2,5-dimethylpiperazine-1-carboxylate, serves as a key building block and intermediate in pharmaceutical and chemical synthesis. The Boc protecting group on the piperazine ring enables selective functionalization and is valuable for constructing enantiomerically pure piperazine-containing molecules, which are common scaffolds in active pharmaceutical ingredients (APIs) for drugs targeting various biological pathways. Its defined stere

This chiral compound, specifically the (2R,5R)-enantiomer of tert-butyl 2,5-dimethylpiperazine-1-carboxylate, serves as a key building block and intermediate in pharmaceutical and chemical synthesis. The Boc protecting group on the piperazine ring enables selective functionalization and is valuable for constructing enantiomerically pure piperazine-containing molecules, which are common scaffolds in active pharmaceutical ingredients (APIs) for drugs targeting various biological pathways. Its defined stereochemistry ensures precise control essential for drug efficacy and safety. The compound's stability and reactivity support its use in multi-step organic syntheses aimed at developing novel therapeutics.

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