885588-12-5 | 2-Bromo-5-fluoroisonicotinic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	99%	in stock	$10.00	$7.00
5g	98%	in stock	$35.00	$24.00
10g	98%	in stock	$50.00	$35.00
25g	98%	in stock	$124.00	$87.00
100g	99%	in stock	$480.00	$336.00

Description

• Catalog Number: AC04684
• Chemical Name: 2-Bromo-5-fluoroisonicotinic acid
• CAS Number: 885588-12-5
• Molecular Formula: C6H3BrFNO2
• Molecular Weight: 219.9959
• MDL Number: MFCD18426717
• SMILES: Brc1ncc(c(c1)C(=O)O)F

Computed Properties

• Complexity: 167
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.5

Upstream Synthesis Route

2-Bromo-5-fluoroisonicotinic acid is a valuable chemical compound widely used in chemical synthesis due to its unique properties and reactivity. As a versatile building block, this compound is often utilized in the synthesis of pharmaceuticals, agrochemicals, and other specialized chemicals. Its strategic incorporation into organic molecules can impart specific biological activities or structural features, making it an important intermediate in various research and industrial applications.One of the key applications of 2-Bromo-5-fluoroisonicotinic acid is in the preparation of heterocyclic compounds, particularly in the synthesis of pyridine derivatives. By leveraging its bromo and fluoro substituents, chemists can efficiently introduce functional groups at specific positions within the pyridine ring, allowing for the creation of diverse molecular structures with desired properties. This compound's ability to participate in cross-coupling reactions, such as Suzuki or Heck coupling, further enhances its utility in building complex molecular scaffolds.Additionally, 2-Bromo-5-fluoroisonicotinic acid serves as a valuable reagent for the synthesis of novel drug candidates and pharmacophores. Its structural features can be fine-tuned to modulate the pharmacological properties of target compounds, enabling medicinal chemists to explore new avenues in drug discovery and development. Furthermore, its compatibility with various synthetic methodologies enables rapid access to analogs and derivatives for structure-activity relationship studies and lead optimization.Overall, the use of 2-Bromo-5-fluoroisonicotinic acid in chemical synthesis offers a powerful tool for designing and accessing a wide range of molecular architectures with potential applications in pharmaceuticals, agrochemicals, and materials science. Its versatility and reactivity make it a valuable resource for synthetic chemists seeking to innovate and advance their research in the field of organic chemistry.