4-(3-Nitro-pyridin-2-yloxy)-piperidine-1-carboxylicacidtert-butylester

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Reagent Code: #219575
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CAS Number 1065484-06-1

science Other reagents with same CAS 1065484-06-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.344 g/mol
Formula C₁₅H₂₁N₃O₅
badge Registry Numbers
MDL Number MFCD09877660
thermostat Physical Properties
Boiling Point 442.0±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.247 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 biologically active compounds. Its structure supports the construction of complex molecules with potential activity in oncology and inflammatory diseases. The tert-butyl ester group allows for selective deprotection, enabling stepwise synthesis in multi-stage drug manufacturing. Commonly employed in medicinal chemistry for modifying solubility and bioavailability during lead optimization.

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inventory 500mg
10-20 days ฿29,360.00

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4-(3-Nitro-pyridin-2-yloxy)-piperidine-1-carboxylicacidtert-butylester
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of complex molecules with potential activity in oncology and inflammatory diseases. The tert-butyl ester group allows for selective deprotection, enabling stepwise synthesis in multi-stage drug manufacturing. Commonly employed in medicinal chemistry for modifying solubility and bioavailability during lead optimization.
Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of complex molecules with potential activity in oncology and inflammatory diseases. The tert-butyl ester group allows for selective deprotection, enabling stepwise synthesis in multi-stage drug manufacturing. Commonly employed in medicinal chemistry for modifying solubility and bioavailability during lead optimization.
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