tert-Butyl 4-(2-cyanobenzyl)piperazine-1-carboxylate

95%

Reagent Code: #131015
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CAS Number 2703756-90-3

science Other reagents with same CAS 2703756-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.38 g/mol
Formula C₁₇H₂₃N₃O₂
badge Registry Numbers
MDL Number MFCD31716077
thermostat Physical Properties
Boiling Point 412.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that target central nervous system disorders. Its structure allows for the introduction of piperazine-based motifs, which are common in drugs with antipsychotic, antidepressant, or antihistaminic activity. The cyano group enables further chemical transformations, such as reduction to aminomethyl or conversion to heterocycles, making it valuable in medicinal chemistry for building complex molecules. Also employed in research settings for library generation in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,020.00
inventory 1g
10-20 days ฿7,370.00
tert-Butyl 4-(2-cyanobenzyl)piperazine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that target central nervous system disorders. Its structure allows for the introduction of piperazine-based motifs, which are common in drugs with antipsychotic, antidepressant, or antihistaminic activity. The cyano group enables further chemical transformations, such as reduction to aminomethyl or conversion to heterocycles, making it valuable in medicinal chemis
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that target central nervous system disorders. Its structure allows for the introduction of piperazine-based motifs, which are common in drugs with antipsychotic, antidepressant, or antihistaminic activity. The cyano group enables further chemical transformations, such as reduction to aminomethyl or conversion to heterocycles, making it valuable in medicinal chemistry for building complex molecules. Also employed in research settings for library generation in drug discovery programs.
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