tert-Butyl 4-nitro-1H-pyrazole-1-carboxylate

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Reagent Code: #140825
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CAS Number 1018446-96-2

science Other reagents with same CAS 1018446-96-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.19 g/mol
Formula C₈H₁₁N₃O₄
badge Registry Numbers
MDL Number MFCD26401544
thermostat Physical Properties
Boiling Point 319.5±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.32±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a protected pyrazole derivative in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group stabilizes the pyrazole ring during multi-step reactions, allowing selective functionalization at other sites. After desired transformations, the Boc group can be easily removed under mild acidic conditions to liberate the parent pyrazole, making it valuable in the development of bioactive molecules. It is also employed in the synthesis of kinase inhibitors and other heterocyclic compounds with biological activity.

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inventory 1g
10-20 days ฿1,280.00

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tert-Butyl 4-nitro-1H-pyrazole-1-carboxylate
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Used as a protected pyrazole derivative in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group stabilizes the pyrazole ring during multi-step reactions, allowing selective functionalization at other sites. After desired transformations, the Boc group can be easily removed under mild acidic conditions to liberate the parent pyrazole, making it valuable in the development of bioactive molecules. It is also employed in the synthesis of kinase inh

Used as a protected pyrazole derivative in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group stabilizes the pyrazole ring during multi-step reactions, allowing selective functionalization at other sites. After desired transformations, the Boc group can be easily removed under mild acidic conditions to liberate the parent pyrazole, making it valuable in the development of bioactive molecules. It is also employed in the synthesis of kinase inhibitors and other heterocyclic compounds with biological activity.

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