(1-Propyl-1H-pyrazol-4-yl)boronic acid

95%

Reagent Code: #89493
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CAS Number 847818-57-9

science Other reagents with same CAS 847818-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.98 g/mol
Formula C₆H₁₁BN₂O₂
badge Registry Numbers
MDL Number MFCD11504862
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(1-Propyl-1H-pyrazol-4-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the synthesis of various biologically active compounds, including potential drug candidates. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides, making it valuable in the development of new therapeutic agents and advanced materials. Additionally, it may be utilized in the preparation of functionalized pyrazole derivatives, which are often explored for their pharmacological properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿783.00
inventory 1g
10-20 days ฿1,908.00
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(1-Propyl-1H-pyrazol-4-yl)boronic acid
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(1-Propyl-1H-pyrazol-4-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the synthesis of various biologically active compounds, including potential drug candidates. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides, making it valuable in the development of new therapeutic agents and advanced materials. Additionally, it may be utilized in the preparation of functionalized pyrazole derivatives, which are often explored for their pharmacological properties.
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