(R)-tert-Butyl2-(cyanomethyl)piperazine-1-carboxylate

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Reagent Code: #231974
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CAS Number 2387560-41-8

science Other reagents with same CAS 2387560-41-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.29 g/mol
Formula C₁₁H₁₉N₃O₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of selective receptor modulators. Its piperazine core with a cyanomethyl group enables structural diversity for drug design, especially in central nervous system agents and kinase inhibitors. The tert-butoxycarbonyl (Boc) protection allows for controlled deprotection and further functionalization in multi-step syntheses. The (R)-configuration is crucial for enantioselective activity in target binding, making it valuable in asymmetric synthesis of active pharmaceutical ingredients (APIs).

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,470.00
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(R)-tert-Butyl2-(cyanomethyl)piperazine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of selective receptor modulators. Its piperazine core with a cyanomethyl group enables structural diversity for drug design, especially in central nervous system agents and kinase inhibitors. The tert-butoxycarbonyl (Boc) protection allows for controlled deprotection and further functionalization in multi-step syntheses. The (R)-configuration is crucial for enantioselective activity

Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of selective receptor modulators. Its piperazine core with a cyanomethyl group enables structural diversity for drug design, especially in central nervous system agents and kinase inhibitors. The tert-butoxycarbonyl (Boc) protection allows for controlled deprotection and further functionalization in multi-step syntheses. The (R)-configuration is crucial for enantioselective activity in target binding, making it valuable in asymmetric synthesis of active pharmaceutical ingredients (APIs).

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