(S)-tert-Butyl 3-(cyanomethyl)piperazine-1-carboxylate

97%

Reagent Code: #235924
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CAS Number 1589082-06-3

science Other reagents with same CAS 1589082-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.29 g/mol
Formula C₁₁H₁₉N₃O₂
badge Registry Numbers
MDL Number MFCD31978023
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly pharmaceuticals. Its piperazine core with a chiral center and functional groups allows for selective reactions in drug development. Commonly employed in the preparation of kinase inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocycle synthesis, enabling controlled deprotection and further derivatization. The cyanomethyl moiety can be transformed into carboxylic acids, amines, or tetrazoles, expanding its utility in medicinal chemistry for building diverse molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,430.00
inventory 250mg
10-20 days ฿5,870.00
inventory 1g
10-20 days ฿16,790.00
inventory 5g
10-20 days ฿72,930.00
(S)-tert-Butyl 3-(cyanomethyl)piperazine-1-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly pharmaceuticals. Its piperazine core with a chiral center and functional groups allows for selective reactions in drug development. Commonly employed in the preparation of kinase inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocycle synthesis, enabling controlled deprotection and further derivatization. The cyanomethyl moiety can be transfo

Used as an intermediate in the synthesis of biologically active compounds, particularly pharmaceuticals. Its piperazine core with a chiral center and functional groups allows for selective reactions in drug development. Commonly employed in the preparation of kinase inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocycle synthesis, enabling controlled deprotection and further derivatization. The cyanomethyl moiety can be transformed into carboxylic acids, amines, or tetrazoles, expanding its utility in medicinal chemistry for building diverse molecular architectures.

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