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2-Fluoropyridine CAS:372-48-5

Short Description:

Catalog Number: XD96248
Cas: 372-48-5
Molecular Formula: C5H4FN
Molecular Weight: 97.09
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Product Detail

Product Tags

Catalog Number XD96248
Product Name 2-Fluoropyridine
CAS 372-48-5
Molecular Formula C5H4FN
Molecular Weight 97.09
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

2-Fluoropyridine is a heterocyclic compound with the molecular formula C5H4FN. The addition of a fluorine atom to the pyridine ring can have significant effects on the chemical and physical properties of the compound, leading to various applications.One of the main effects of 2-fluoropyridine is its influence on the compound's reactivity. The presence of the fluorine atom can alter the electronic distribution within the molecule, making it more electron-withdrawing in nature. This change in electron density can affect its reactivity towards different chemical reactions. For example, the presence of the fluorine atom can increase the electrophilicity of the pyridine ring, making it more reactive towards nucleophiles in substitution reactions. This enhanced reactivity can be used in organic synthesis for the introduction of various functional groups or for the production of other derivatives.Another effect of 2-fluoropyridine is its impact on the compound's physical properties. Fluorine substituents are known for their unique electron-withdrawing properties and their ability to affect the lipophilicity of compounds. In the case of 2-fluoropyridine, the fluorine atom can increase its lipophilicity, making it more soluble in nonpolar or organic solvents. This property can be advantageous in applications such as formulation of pharmaceuticals or agrochemicals, where solubility is essential.Furthermore, the presence of the fluorine atom in 2-fluoropyridine can also influence its spectroscopic properties. Fluorine atoms have distinctive NMR and IR spectral features, which can be used for the identification and characterization of the compound in analytical chemistry. The presence of the fluorine atom can result in shifts in NMR signals and changes in IR absorption frequencies, allowing for the determination of the compound's structure and purity.In conclusion, the addition of a fluorine atom to the pyridine ring in 2-fluoropyridine can significantly affect its reactivity, solubility, and spectroscopic properties. These effects make 2-fluoropyridine a versatile compound with potential applications in various fields such as organic synthesis, pharmaceutical development, and chemical research. It can serve as a valuable building block for the synthesis of diverse molecules or as a starting material for the preparation of compounds with enhanced properties.


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    2-Fluoropyridine CAS:372-48-5