(3R,5S)-rel-tert-Butyl 3,5-dimethylpiperazine-1-carboxylate

98%

Reagent Code: #123390
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CAS Number 129779-30-2

science Other reagents with same CAS 129779-30-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.30 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD06795911
thermostat Physical Properties
Boiling Point 279.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperazine ring, makes it valuable for developing drugs that target central nervous system disorders, cardiovascular diseases, and other therapeutic areas. It is often employed in the preparation of compounds with potential anti-inflammatory, antimicrobial, or antiviral properties. Additionally, its tert-butyl and carboxylate groups enhance its stability and reactivity, making it suitable for complex chemical transformations in drug development processes. The compound’s stereochemistry also allows for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects in medicinal applications.

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Test Parameter Specification
Appearance Colorless or white to yellow solid or liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days $14.33
inventory 100mg
10-20 days $10.59
inventory 25g
10-20 days $212.82
inventory 5g
10-20 days $65.12
inventory 1g
10-20 days $21.50

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(3R,5S)-rel-tert-Butyl 3,5-dimethylpiperazine-1-carboxylate
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperazine ring, makes it valuable for developing drugs that target central nervous system disorders, cardiovascular diseases, and other therapeutic areas. It is often employed in the preparation of compounds with potential anti-inflammatory, antimicrobial, or antiviral properties. Additionally, its tert-butyl and carboxylate groups enhance its stability and reactivity, making it suitable for complex chemical transformations in drug development processes. The compound’s stereochemistry also allows for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects in medicinal applications.
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