(1-Methyl-1H-pyrazol-4-yl)boronic acid hydrochloride

98%

Reagent Code: #203032
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CAS Number 1026796-02-0

science Other reagents with same CAS 1026796-02-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.38 g/mol
Formula C₄H₈BClN₂O₂
badge Registry Numbers
MDL Number MFCD09972098
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its pyrazole ring is valuable for constructing active pharmaceutical ingredients (APIs) in drug discovery, especially in development of kinase inhibitors and anti-inflammatory agents. The boronic acid group enables efficient carbon-carbon bond formation, while the hydrochloride salt enhances stability and handling. Commonly employed in research settings for generating novel heterocyclic compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,270.00
inventory 10g
10-20 days ฿14,270.00
(1-Methyl-1H-pyrazol-4-yl)boronic acid hydrochloride
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Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its pyrazole ring is valuable for constructing active pharmaceutical ingredients (APIs) in drug discovery, especially in development of kinase inhibitors and anti-inflammatory agents. The boronic acid group enables efficient carbon-carbon bond formation, while the hydrochloride salt enhances stability and handling. Commonly employed in research settings for generating

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its pyrazole ring is valuable for constructing active pharmaceutical ingredients (APIs) in drug discovery, especially in development of kinase inhibitors and anti-inflammatory agents. The boronic acid group enables efficient carbon-carbon bond formation, while the hydrochloride salt enhances stability and handling. Commonly employed in research settings for generating novel heterocyclic compounds with potential biological activity.

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