[1-(6-Chloro-pyrimidin-4-yl)-piperidin-4-yl]-carbamicacidtert-butylester

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Reagent Code: #164267
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CAS Number 596817-50-4

science Other reagents with same CAS 596817-50-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.795 g/mol
Formula C₁₄H₂₁ClN₄O₂
badge Registry Numbers
MDL Number MFCD09607518
thermostat Physical Properties
Boiling Point 476.7±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.24 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a key role in medicinal chemistry for constructing biologically active molecules targeting inflammatory diseases and certain cancers. The tert-butyl carbamate group protects the amine during synthesis, allowing selective reactions at other sites, while the chloropyrimidine moiety serves as a handle for further coupling reactions. Its structure supports the creation of highly specific drug candidates in research and development settings.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿18,540.00

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[1-(6-Chloro-pyrimidin-4-yl)-piperidin-4-yl]-carbamicacidtert-butylester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a key role in medicinal chemistry for constructing biologically active molecules targeting inflammatory diseases and certain cancers. The tert-butyl carbamate group protects the amine during synthesis, allowing selective reactions at other sites, while the chloropyrimidine moiety serves as a handle for further coupling reactions. Its structure supports the creation of highl

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a key role in medicinal chemistry for constructing biologically active molecules targeting inflammatory diseases and certain cancers. The tert-butyl carbamate group protects the amine during synthesis, allowing selective reactions at other sites, while the chloropyrimidine moiety serves as a handle for further coupling reactions. Its structure supports the creation of highly specific drug candidates in research and development settings.

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