2,6-Difluoro-4-Iodonicotinaldehyde

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Reagent Code: #179016
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CAS Number 2417489-94-0

science Other reagents with same CAS 2417489-94-0

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Weight 268.99 g/mol
Formula C₆H₂F₂INO
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Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. The aldehyde group enables Schiff base formation or reduction to amines, while the iodine atom facilitates cross-coupling reactions such as Suzuki or Heck reactions. The fluorine atoms enhance binding affinity and metabolic stability in final drug candidates. Commonly employed in medicinal chemistry for optimizing lead compounds in oncology and inflammatory disease research.

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inventory 100mg
10-20 days ฿1,940.00

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2,6-Difluoro-4-Iodonicotinaldehyde
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Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. The aldehyde group enables Schiff base formation or reduction to amines, while the iodine atom facilitates cross-coupling reactions such as Suzuki or Heck reactions. The fluorine atoms enhance binding affinity and metabolic stability i

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. The aldehyde group enables Schiff base formation or reduction to amines, while the iodine atom facilitates cross-coupling reactions such as Suzuki or Heck reactions. The fluorine atoms enhance binding affinity and metabolic stability in final drug candidates. Commonly employed in medicinal chemistry for optimizing lead compounds in oncology and inflammatory disease research.

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