2-Methoxy-4-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid

95%

Reagent Code: #91710
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CAS Number 2225169-77-5

science Other reagents with same CAS 2225169-77-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.04352 g/mol
Formula C₁₁H₁₃BN₂O₃
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it finds application in the development of biologically active molecules, such as kinase inhibitors, due to its structural compatibility with drug-like scaffolds. Its pyrazole moiety further enhances its utility in designing compounds with potential therapeutic properties.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿32,760.00

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2-Methoxy-4-(3-methyl-1H-pyrazol-1-yl)phenylboronic acid
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it finds application in the development of biologically active molecules, such as kinase inhibitors, due to its structural compatibilit

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it finds application in the development of biologically active molecules, such as kinase inhibitors, due to its structural compatibility with drug-like scaffolds. Its pyrazole moiety further enhances its utility in designing compounds with potential therapeutic properties.

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