tert-Butyl 2-propylpiperazine-1-carboxylate

98%

Reagent Code: #116012
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CAS Number 1027511-67-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.33 g/mol
Formula C₁₂H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD08273955
thermostat Physical Properties
Boiling Point 303.9±17.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.972±0.06 g/cm3(Predicted)
Storage Room temperature, dark, inert gas

description Product Description

This chemical is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of compounds targeting neurological and psychiatric disorders, such as antipsychotics and antidepressants. Additionally, it serves as a building block in the creation of piperazine derivatives, which are often incorporated into drugs to enhance their pharmacokinetic properties. The tert-butyl group provides steric protection during synthetic processes, ensuring the stability and selectivity of the reactions. Its application is also explored in medicinal chemistry research for the design of novel therapeutic agents with improved efficacy and reduced side effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,971.00
inventory 1g
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿3,339.00
tert-Butyl 2-propylpiperazine-1-carboxylate
This chemical is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of compounds targeting neurological and psychiatric disorders, such as antipsychotics and antidepressants. Additionally, it serves as a building block in the creation of piperazine derivatives, which are often incorporated into drugs to enhance their pharmacokinetic properties. The tert-butyl group provides steric protection during synthetic processes, ensuring the stability and selectivity of the reactions. Its application is also explored in medicinal chemistry research for the design of novel therapeutic agents with improved efficacy and reduced side effects.
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