2-Methyl-5-trifluoromethyl-4-cyclopropylphenylboronic acid

95%

Reagent Code: #91751
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CAS Number 2225170-41-0

science Other reagents with same CAS 2225170-41-0

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Weight 244.0179896 g/mol
Formula C₁₁H₁₂BF₃O₂
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. The trifluoromethyl and cyclopropyl groups enhance its utility in designing molecules with specific biological activities or chemical properties. It is often employed in the development of drug candidates, where its structural features contribute to improved stability, bioavailability, or target specificity. Additionally, it finds applications in material science for synthesizing advanced organic materials with tailored functionalities.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿27,900.00

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2-Methyl-5-trifluoromethyl-4-cyclopropylphenylboronic acid
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. The trifluoromethyl and cyclopropyl groups enhance its utility in designing molecules with specific biological activities or

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. The trifluoromethyl and cyclopropyl groups enhance its utility in designing molecules with specific biological activities or chemical properties. It is often employed in the development of drug candidates, where its structural features contribute to improved stability, bioavailability, or target specificity. Additionally, it finds applications in material science for synthesizing advanced organic materials with tailored functionalities.

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