2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)aniline
98%
Reagent
Code: #243221
CAS Number
1196972-92-5
science Other reagents with same CAS 1196972-92-5
blur_circular Chemical Specifications
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Molecular Information
Weight
287.09 g/mol
Formula
C₁₃H₁₇BF₃NO₂
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Registry Numbers
MDL Number
MFCD16996232
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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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