2-Trifluoromethyl-4-(1H-pyrazol-1-yl)phenylboronic acid

95%

Reagent Code: #91776
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CAS Number 2225155-29-1

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Weight 255.9889296 g/mol
Formula C₁₀H₈BF₃N₂O₂
inventory_2 Storage & Handling
Storage -20℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting inflammation and cancer. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic chemistry to form carbon-carbon bonds. This makes it valuable in creating complex molecules for medicinal chemistry. Additionally, it is employed in the production of agrochemicals, where its trifluoromethyl and pyrazole groups contribute to the biological activity of the final compounds. Its unique structure also makes it useful in material science, particularly in the design of advanced polymers and coatings with specific properties.

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inventory 25mg
10-20 days ฿32,760.00

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2-Trifluoromethyl-4-(1H-pyrazol-1-yl)phenylboronic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting inflammation and cancer. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic chemistry to form carbon-carbon bonds. This makes it valuable in creating complex molecules for medicinal chemistry. Additionally, it is employed in the production of agrochemicals, where its trifluoromethyl and pyrazole groups contribute to th

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting inflammation and cancer. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic chemistry to form carbon-carbon bonds. This makes it valuable in creating complex molecules for medicinal chemistry. Additionally, it is employed in the production of agrochemicals, where its trifluoromethyl and pyrazole groups contribute to the biological activity of the final compounds. Its unique structure also makes it useful in material science, particularly in the design of advanced polymers and coatings with specific properties.

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