(1-(tert-Butyl)-1H-pyrazol-4-yl)boronic acid

≥98%

Reagent Code: #192620
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CAS Number 1416785-99-3

science Other reagents with same CAS 1416785-99-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168 g/mol
Formula C₇H₁₃BN₂O₂
badge Registry Numbers
MDL Number MFCD18250635
thermostat Physical Properties
Boiling Point 320.3±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.08±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and agrochemicals. Its pyrazole ring system contributes to biological activity, making it valuable in drug discovery, particularly in the development of kinase inhibitors and anti-inflammatory agents. The boronic acid group allows for efficient carbon-carbon bond formation under mild conditions, enabling the construction of complex heterocyclic compounds. Commonly employed in medicinal chemistry for library synthesis and structure-activity relationship studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,760.00
inventory 250mg
10-20 days ฿4,510.00
inventory 1g
10-20 days ฿9,600.00

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(1-(tert-Butyl)-1H-pyrazol-4-yl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and agrochemicals. Its pyrazole ring system contributes to biological activity, making it valuable in drug discovery, particularly in the development of kinase inhibitors and anti-inflammatory agents. The boronic acid group allows for efficient carbon-carbon bond formation under mild conditions, enabling the construction of complex heterocyclic compounds. Commonly employed in medicinal chemistry for library synthesis and structure-activity relationship studies.
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