5-Bromo-6-(3-methyl-1H-pyrazol-1-yl)pyridine-3-boronic acid

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Reagent Code: #92301
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CAS Number 2225155-10-0

science Other reagents with same CAS 2225155-10-0

blur_circular Chemical Specifications

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Weight 281.90166 g/mol
Formula C₉H₉BBrN₃O₂
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating biaryl structures, which are common in active pharmaceutical ingredients. Additionally, the pyrazole moiety in its structure contributes to its application in designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Its versatility makes it a useful intermediate in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿12,492.00
inventory 25mg
10-20 days ฿29,592.00

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5-Bromo-6-(3-methyl-1H-pyrazol-1-yl)pyridine-3-boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating biaryl structures, which are common in active pharmaceutical ingredients. Additionally, the pyrazole moiety in its structure contributes to its

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating biaryl structures, which are common in active pharmaceutical ingredients. Additionally, the pyrazole moiety in its structure contributes to its application in designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Its versatility makes it a useful intermediate in drug discovery and development processes.

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