1218790-66-9 | 2-Ethoxy-5-(trifluoromethyl)pyridine-3-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$58.00	$40.00
1g	95%	in stock	$105.00	$74.00
5g	95%	in stock	$409.00	$286.00
10g	95%	in stock	$665.00	$466.00
25g	95%	in stock	$1,317.00	$922.00
100g	95%	in stock	$3,743.00	$2,620.00

Description

• Catalog Number: AA54570
• Chemical Name: 2-Ethoxy-5-(trifluoromethyl)pyridine-3-boronic acid
• CAS Number: 1218790-66-9
• Molecular Formula: C8H9BF3NO3
• Molecular Weight: 234.9682
• MDL Number: MFCD15143470
• SMILES: CCOc1ncc(cc1B(O)O)C(F)(F)F

Upstream Synthesis Route

(2-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid is a versatile chemical reagent widely used in chemical synthesis for its unique properties and applications. This boronic acid derivative is particularly valued for its ability to serve as a key building block in the construction of complex organic molecules through Suzuki-Miyaura cross-coupling reactions.In organic synthesis, Suzuki-Miyaura cross-coupling reactions are vital transformations that involve the coupling of an organoboron compound, such as (2-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid, with an organic halide or pseudohalide. By utilizing this boronic acid derivative as a coupling partner, chemists can introduce the pyridine and trifluoromethyl functional groups into target molecules with precision and efficiency.The presence of the ethoxy and trifluoromethyl substituents on the pyridine ring not only imparts unique reactivity to the boronic acid but also allows for further derivatization, enabling the synthesis of a diverse array of heterocyclic and fluorinated compounds. This versatility makes (2-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid a valuable tool in medicinal chemistry, materials science, and agrochemical research, where the design and synthesis of novel molecular structures are essential.Whether utilized for the incorporation of specific functional groups, the preparation of pharmaceutical intermediates, or the modification of natural products, (2-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid stands out as a crucial reagent in the toolbox of synthetic chemists aiming to access diverse and complex molecules with high efficiency and selectivity.