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Sku CI27045_250_G
Chem Impex
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Product Information

Product Name
3-Fluoropyridine
Brand Name
Chem Impex
Product Number
27045
CAS
372-47-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
67794
IUPAC Name
3-fluoropyridine
InChI Key
CELKOWQJPVJKIL-UHFFFAOYSA-N
SMILES
C1=CC(=CN=C1)F

Application

3-Fluoropyridine is widely utilized in research focused on:

Pharmaceutical Development: It serves as a key intermediate in the synthesis of various pharmaceuticals, including anti-inflammatory and anti-cancer drugs, enhancing therapeutic efficacy.

Agricultural Chemicals: This compound is used in the formulation of agrochemicals, contributing to the development of new pesticides and herbicides that improve crop yield and pest resistance.

Material Science: It plays a role in the production of advanced materials, such as polymers and coatings, which offer improved durability and chemical resistance.

Organic Synthesis: Researchers leverage its reactivity in organic synthesis to create complex molecules, facilitating advancements in chemical research and innovation.

Analytical Chemistry: It is utilized as a standard in analytical methods, aiding in the detection and quantification of other compounds in various samples, ensuring accuracy in research findings.

References

Unmasking the reverse catalytic activity of ‘ene’-reductases for asymmetric carbonyl desaturation

Publication Name: Nature Chemistry
Publication Date: 2024-11-26
DOI: 10.1038/s41557-024-01671-1

Overview of Highly Solvating Electrolytes for Lean Electrolyte Conditions in Lithium–Sulfur Batteries

Publication Name: Korean Journal of Chemical Engineering
Publication Date: 2024-02
DOI: 10.1007/s11814-024-00103-7

The applications of organozinc reagents in continuous flow chemistry: Negishi coupling

Publication Name: Journal of Flow Chemistry
Publication Date: 2023-01-12
DOI: 10.1007/s41981-022-00253-x

Alkenylation with Alkynes

Publication Name: Science of Synthesis
Publication Date: 2022

A directive Ni catalyst overrides conventional site selectivity in pyridine C–H alkenylation

Publication Name: Nature Chemistry
Publication Date: 2021-10-11
DOI: 10.1038/s41557-021-00792-1