4-(4-Cyano-pyridin-2-yl)-piperazine-1-carboxylicacidtert-butylester

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Reagent Code: #164260
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CAS Number 884507-31-7

science Other reagents with same CAS 884507-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.345 g/mol
Formula C₁₅H₂₀N₄O₂
badge Registry Numbers
MDL Number MFCD08741437
thermostat Physical Properties
Melting Point 127 °C
Boiling Point 439.9 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.21 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective modification, making it valuable in creating compounds with high target specificity. Commonly employed in medicinal chemistry for constructing drug candidates targeting neurological disorders and cancer. The tert-butyl ester group facilitates protection during multi-step synthesis, while the cyano-pyridinyl moiety contributes to binding affinity in receptor interactions.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿21,000.00

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4-(4-Cyano-pyridin-2-yl)-piperazine-1-carboxylicacidtert-butylester
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective modification, making it valuable in creating compounds with high target specificity. Commonly employed in medicinal chemistry for constructing drug candidates targeting neurological disorders and cancer. The tert-butyl ester group facilitates protection during multi-step synthesis, while the cyano-pyridinyl moiety contributes to bindin

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective modification, making it valuable in creating compounds with high target specificity. Commonly employed in medicinal chemistry for constructing drug candidates targeting neurological disorders and cancer. The tert-butyl ester group facilitates protection during multi-step synthesis, while the cyano-pyridinyl moiety contributes to binding affinity in receptor interactions.

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