tert-Butyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)-7-azaspiro[3.5]nonane-7-carboxylate

Reagent Code: #141093
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CAS Number 2304635-20-7

science Other reagents with same CAS 2304635-20-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 417.3499 g/mol
Formula C₂₂H₃₆BN₃O₄
thermostat Physical Properties
Boiling Point 536.0±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily in pharmaceutical research and development as an intermediate in the synthesis of biologically active compounds. Its structure supports the construction of complex molecules through cross-coupling reactions, particularly Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. The presence of the pyrazole ring and the spirocyclic framework makes it valuable in designing kinase inhibitors and other targeted therapies. The tert-butyl carbamate (Boc) group provides protection for the nitrogen during multi-step syntheses, allowing selective deprotection under mild conditions. This compound is especially useful in medicinal chemistry for developing drug candidates within oncology and central nervous system disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,210.00
inventory 500mg
10-20 days ฿36,320.00

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tert-Butyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)-7-azaspiro[3.5]nonane-7-carboxylate
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Used primarily in pharmaceutical research and development as an intermediate in the synthesis of biologically active compounds. Its structure supports the construction of complex molecules through cross-coupling reactions, particularly Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. The presence of the pyrazole ring and the spirocyclic framework makes it valuable in designing kinase inhibitors and other targeted therapies. The tert-butyl carbamate (Boc) group provides protection f

Used primarily in pharmaceutical research and development as an intermediate in the synthesis of biologically active compounds. Its structure supports the construction of complex molecules through cross-coupling reactions, particularly Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. The presence of the pyrazole ring and the spirocyclic framework makes it valuable in designing kinase inhibitors and other targeted therapies. The tert-butyl carbamate (Boc) group provides protection for the nitrogen during multi-step syntheses, allowing selective deprotection under mild conditions. This compound is especially useful in medicinal chemistry for developing drug candidates within oncology and central nervous system disorders.

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