(1H-Pyrazol-3-yl)boronic acid hydrochloride

97%

Reagent Code: #195657
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CAS Number 1314216-33-5

science Other reagents with same CAS 1314216-33-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 148.36 g/mol
Formula C₃H₆BClN₂O₂
badge Registry Numbers
MDL Number MFCD21091124
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid functionality enables the formation of carbon-carbon bonds, making it valuable in drug discovery for constructing heterocyclic frameworks. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to the prevalence of pyrazole motifs in medicinal chemistry. The hydrochloride salt enhances stability and handling during synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,780.00
1g
10-20 days ฿4,430.00
5g
10-20 days ฿16,560.00
(1H-Pyrazol-3-yl)boronic acid hydrochloride
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid functionality enables the formation of carbon-carbon bonds, making it valuable in drug discovery for constructing heterocyclic frameworks. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to the prevalence of pyrazole motifs in medicinal chemistry. The hydrochloride salt enhances s

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid functionality enables the formation of carbon-carbon bonds, making it valuable in drug discovery for constructing heterocyclic frameworks. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to the prevalence of pyrazole motifs in medicinal chemistry. The hydrochloride salt enhances stability and handling during synthesis.

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