1227578-23-5 | 4-Bromo-6-fluoropyridin-3-ol

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$210.00	$147.00
250mg	95%	in stock	$303.00	$212.00
1g	95%	in stock	$759.00	$531.00

Description

• Catalog Number: AA24852
• Chemical Name: 4-Bromo-6-fluoropyridin-3-ol
• CAS Number: 1227578-23-5
• Molecular Formula: C5H3BrFNO
• Molecular Weight: 191.9858
• MDL Number: MFCD16609914
• SMILES: Fc1ncc(c(c1)Br)O

Upstream Synthesis Route

4-Bromo-6-fluoropyridin-3-ol, also known as $name$, is a versatile chemical compound widely used in chemical synthesis for its unique properties and reactivity. This compound plays a crucial role in various organic reactions and serves as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and numerous other fine chemicals.One key application of 4-Bromo-6-fluoropyridin-3-ol is in the formation of heterocyclic compounds. By undergoing substitution reactions at the bromo and fluorine positions, this compound can be functionalized to introduce a wide range of additional functional groups, allowing for the creation of complex molecular structures. These heterocyclic compounds are of significant interest in medicinal chemistry and material science due to their diverse biological activities and unique properties.Additionally, 4-Bromo-6-fluoropyridin-3-ol is commonly employed in transition metal-catalyzed cross-coupling reactions. The bromo and fluorine substituents on the pyridine ring serve as reactive sites for coupling with various organic electrophiles or nucleophiles under appropriate catalytic conditions. This enables the rapid and efficient construction of carbon-carbon and carbon-heteroatom bonds, which are essential for the synthesis of diverse organic molecules.Furthermore, the presence of both bromine and fluorine atoms in 4-Bromo-6-fluoropyridin-3-ol provides opportunities for site-selective functionalization in complex molecule synthesis. The differential reactivity of these halogen substituents allows for precise control over regioselectivity and can facilitate the installation of specific functional groups at desired positions within the molecular framework. This fine-tuned reactivity makes 4-Bromo-6-fluoropyridin-3-ol a valuable tool for chemists seeking to tailor the structure and properties of organic compounds for various applications.In conclusion, 4-Bromo-6-fluoropyridin-3-ol is a versatile and valuable compound in chemical synthesis due to its reactivity, functional group tolerance, and potential for site-selective modification. Its applications in heterocyclic synthesis, cross-coupling reactions, and site-selective functionalization make it an indispensable building block for the development of novel molecules with diverse properties and applications in the fields of pharmaceuticals, agrochemicals, and materials science.