1072946-62-3 | 2-Methoxy-3-(trifluoromethyl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$129.00	$90.00
250mg	95%	in stock	$171.00	$120.00
1g	95%	in stock	$356.00	$249.00
5g	95%	in stock	$946.00	$662.00

Description

• Catalog Number: AE08171
• Chemical Name: 2-Methoxy-3-(trifluoromethyl)phenylboronic acid
• CAS Number: 1072946-62-3
• Molecular Formula: C8H8BF3O3
• Molecular Weight: 219.9535
• MDL Number: MFCD07772004
• SMILES: COc1c(cccc1C(F)(F)F)B(O)O

Upstream Synthesis Route

(2-Methoxy-3-(trifluoromethyl)phenyl)boronic acid, also known as $name$, is a valuable chemical reagent extensively utilized in organic synthesis. This compound serves as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity. In chemical synthesis, (2-Methoxy-3-(trifluoromethyl)phenyl)boronic acid acts as a key component in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This reaction is widely employed in the construction of complex molecular structures by connecting different functional groups together. By enabling the selective coupling of aryl or heteroaryl halides with boronic acids, this compound allows chemists to efficiently assemble intricate organic compounds with high precision.Furthermore, (2-Methoxy-3-(trifluoromethyl)phenyl)boronic acid can also participate in other transformative reactions such as palladium-catalyzed arylation, borylation, and various metal-catalyzed transformations. Its trifluoromethyl and methoxy substituents provide enhanced electronic properties and steric effects, making it a valuable tool for fine-tuning the reactivity and selectivity of organic reactions.Overall, the application of (2-Methoxy-3-(trifluoromethyl)phenyl)boronic acid in chemical synthesis enables the efficient construction of diverse molecular structures with implications in drug discovery, material science, and beyond.