Ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetate

97%

Reagent Code: #182771
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CAS Number 864754-16-5

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.13 g/mol
Formula C₁₃H₂₁BN₂O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyrazole ring and boronate ester group make it valuable for constructing biologically active molecules, particularly in drug discovery. The ethyl ester functionality allows for further chemical modifications, such as hydrolysis or amidation, to tune solubility or reactivity in multistep organic syntheses. Commonly employed in the development of kinase inhibitors and other heterocyclic compounds with therapeutic potential.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿790.00
1g
10-20 days ฿1,360.00
5g
10-20 days ฿5,980.00
25g
10-20 days ฿23,450.00
Ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetate
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyrazole ring and boronate ester group make it valuable for constructing biologically active molecules, particularly in drug discovery. The ethyl ester functionality allows for further chemical modifications, such as hydrolysis or amidation, to tune solubility or reactivity in multistep organic syntheses. Commonly employed in the developmen

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyrazole ring and boronate ester group make it valuable for constructing biologically active molecules, particularly in drug discovery. The ethyl ester functionality allows for further chemical modifications, such as hydrolysis or amidation, to tune solubility or reactivity in multistep organic syntheses. Commonly employed in the development of kinase inhibitors and other heterocyclic compounds with therapeutic potential.

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