2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)aniline

98%

Reagent Code: #243221
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CAS Number 1196972-92-5

science Other reagents with same CAS 1196972-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.09 g/mol
Formula C₁₃H₁₇BF₃NO₂
badge Registry Numbers
MDL Number MFCD16996232
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. The presence of a trifluoromethyl group enhances the lipophilicity and metabolic stability of target molecules, which is particularly beneficial in drug design. It is also employed in the development of functional materials, including organic semiconductors and fluorescent probes, due to its electronic properties and structural versatility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,300.00
inventory 250mg
10-20 days ฿2,180.00
inventory 5g
10-20 days ฿25,970.00
inventory 1g
10-20 days ฿5,890.00

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2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)aniline
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Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. The presence of a trifluoromethyl group enhances the lipophilicity and metabolic stability of target molecules, which is particularly beneficial in drug design. It is also employed in the development of functional materials, including organic semiconductors and fluorescent probes, due to its electronic properties and structural versatility.
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