(1,3,5-Trimethyl-1H-pyrazol-4-yl)boronic acid

96%

Reagent Code: #241699
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CAS Number 847818-62-6

science Other reagents with same CAS 847818-62-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.98 g/mol
Formula C₆H₁₁BN₂O₂
badge Registry Numbers
MDL Number MFCD11183310
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of kinase inhibitors and other biologically active compounds. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in drug development. Commonly employed in the synthesis of anti-inflammatory, anticancer, and antidiabetic agents due to its stability and reactivity profile. Also utilized in the design of novel heterocyclic compounds where the pyrazole ring acts as a bioisostere for amide or ester functionalities.

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Test Parameter Specification
Appearance White Solid
Purity (%) 95.5-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿412.50
inventory 250mg
10-20 days ฿660.00
inventory 1g
10-20 days ฿2,470.00
inventory 5g
10-20 days ฿10,180.00

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(1,3,5-Trimethyl-1H-pyrazol-4-yl)boronic acid
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Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of kinase inhibitors and other biologically active compounds. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in drug development. Commonly employed in the synthesis of anti-inflammatory, anticancer, and antidiabetic agents due to its stability and reactivity profile. Also utilized in the design of novel heterocyclic compounds where t

Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of kinase inhibitors and other biologically active compounds. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in drug development. Commonly employed in the synthesis of anti-inflammatory, anticancer, and antidiabetic agents due to its stability and reactivity profile. Also utilized in the design of novel heterocyclic compounds where the pyrazole ring acts as a bioisostere for amide or ester functionalities.

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