2-(4-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)phenyl)-1,1,1-trifluoropropan-2-ol

97%

Reagent Code: #115712
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CAS Number 1467061-57-9

science Other reagents with same CAS 1467061-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.10 g/mol
Formula C₁₄H₁₈BF₃O₃
badge Registry Numbers
MDL Number MFCD28133801
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex organic molecules.

In medicinal chemistry, it is often used to create biologically active compounds, including potential drug candidates targeting various diseases. The trifluoromethyl group in its structure enhances the metabolic stability and bioavailability of the resulting molecules, making it advantageous in drug design.

Additionally, its application extends to materials science, where it contributes to the synthesis of advanced polymers and organic electronic materials. The unique combination of boronic ester and trifluoromethyl groups allows for the creation of materials with tailored properties, such as improved thermal stability and electronic conductivity.

Overall, this chemical serves as a versatile building block in both life sciences and material sciences, enabling the development of innovative solutions in drug discovery and advanced material design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,541.00
inventory 100mg
10-20 days ฿8,775.00

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2-(4-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)phenyl)-1,1,1-trifluoropropan-2-ol
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This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex organic molecules.

In medicinal chemistry, it is often used to create biologically active compounds, including potential drug candidates targeting various diseases. The trifluoromethyl group in its str

This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex organic molecules.

In medicinal chemistry, it is often used to create biologically active compounds, including potential drug candidates targeting various diseases. The trifluoromethyl group in its structure enhances the metabolic stability and bioavailability of the resulting molecules, making it advantageous in drug design.

Additionally, its application extends to materials science, where it contributes to the synthesis of advanced polymers and organic electronic materials. The unique combination of boronic ester and trifluoromethyl groups allows for the creation of materials with tailored properties, such as improved thermal stability and electronic conductivity.

Overall, this chemical serves as a versatile building block in both life sciences and material sciences, enabling the development of innovative solutions in drug discovery and advanced material design.

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