100202-78-6 | 2-(Bromomethyl)-6-fluoropyridine

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$15.00	$11.00
250mg	95%	in stock	$25.00	$18.00
1g	95%	in stock	$84.00	$59.00
5g	95%	in stock	$377.00	$264.00
10g	95%	in stock	$565.00	$396.00
25g	95%	in stock	$1,399.00	$980.00

Description

• Catalog Number: AA01415
• Chemical Name: 2-(Bromomethyl)-6-fluoropyridine
• CAS Number: 100202-78-6
• Molecular Formula: C6H5BrFN
• Molecular Weight: 190.01300319999999
• MDL Number: MFCD09953532
• SMILES: BrCc1cccc(n1)F

Upstream Synthesis Route

2-(Bromomethyl)-6-fluoropyridine is a versatile chemical reagent commonly used in organic synthesis applications. Its unique structure allows it to participate in a variety of reactions, making it a valuable tool for chemists in the laboratory.One important application of 2-(Bromomethyl)-6-fluoropyridine is its role as a reactive intermediate in the synthesis of pharmaceutical compounds. By incorporating this compound into a synthetic route, chemists can introduce both bromine and fluorine functionalities into target molecules, enhancing their biological activity and pharmacological properties.Furthermore, 2-(Bromomethyl)-6-fluoropyridine can be utilized in the preparation of complex organic molecules through cross-coupling reactions with various nucleophiles. Its reactivity towards nucleophilic substitution allows for the selective modification of specific positions within a molecule, enabling the synthesis of diverse chemical structures with high precision.In addition, 2-(Bromomethyl)-6-fluoropyridine serves as a key building block for the construction of heterocyclic frameworks, which are prevalent in many pharmaceuticals and agrochemicals. Its ability to undergo cyclization reactions under mild conditions expands the synthetic possibilities for chemists aiming to access a broad range of bioactive compounds.Overall, the inclusion of 2-(Bromomethyl)-6-fluoropyridine in chemical synthesis endeavors offers chemists a powerful tool for the efficient and strategic construction of complex molecular architectures with diverse functional groups.