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Product Information

Product Name
2-Fluoro-4-iodopyridine
Brand Name
Chem Impex
Product Number
28675
CAS
22282-70-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7023570
IUPAC Name
2-fluoro-4-iodopyridine
InChI Key
ADPRIAVYIGHFSO-UHFFFAOYSA-N
SMILES
C1=CN=C(C=C1I)F

Description

2-Fluoro-4-iodopyridine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its unique halogen substitutions enhance biological activity.

Agricultural Chemistry: It is used in the formulation of agrochemicals, including pesticides and herbicides, where its fluorine and iodine atoms contribute to improved efficacy and stability of the active ingredients.

Material Science: The compound is explored in the creation of novel materials, such as conductive polymers and organic semiconductors, due to its electronic properties that facilitate charge transport.

Organic Synthesis: As a versatile building block, it is employed in various organic reactions, including cross-coupling reactions, allowing chemists to create complex molecular architectures efficiently.

Research in Fluorinated Compounds: It plays a significant role in studies aimed at understanding the behavior of fluorinated compounds in biological systems, helping researchers design safer and more effective chemical entities.

References Data Source From Pubchem

Homogeneous Catalyzed Aryl–Aryl Cross-Couplings in Flow

Publication Name: Synthesis
Publication Date: 2021-02-18
DOI: 10.1055/a-1360-7798

Recent Applications of Continuous Flow in Homogeneous Palladium Catalysis

Publication Name: Synthesis
Publication Date: 2020-08-03
DOI: 10.1055/s-0040-1707212

Synthesis of a GDC-0994 Intermediate by Kumada–Corriu Cross-Coupling

Publication Name: Synfacts
Publication Date: 2017-11-17
DOI: 10.1055/s-0036-1591622

N-Nucleophiles

Publication Name: Science of Synthesis
Publication Date: 2016

Reactions of Primary Arylamines with Hetaryl Electrophiles

Publication Name: Science of Synthesis
Publication Date: 2012