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Home  > 3-Fluoro-4-(trifluoromethyl)pyridin-2-amine

AV17036

1227514-27-3 | 3-Fluoro-4-(trifluoromethyl)pyridin-2-amine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $14.00 $10.00 -   +
250mg 97% in stock $25.00 $18.00 -   +
1g 97% in stock $73.00 $51.00 -   +
5g 97% in stock $121.00 $85.00 -   +
10g 97% in stock $241.00 $169.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AV17036
Chemical Name: 3-Fluoro-4-(trifluoromethyl)pyridin-2-amine
CAS Number: 1227514-27-3
Molecular Formula: C6H4F4N2
Molecular Weight: 180.103
MDL Number: MFCD16606170
SMILES: Nc1nccc(c1F)C(F)(F)F

 

Upstream Synthesis Route
  • 3-Fluoro-4-(trifluoromethyl)pyridin-2-amine is a highly versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its incorporation into organic molecules can impart desirable traits such as improved biological activity and enhanced stability.In chemical synthesis, 3-Fluoro-4-(trifluoromethyl)pyridin-2-amine acts as a key intermediate in the construction of complex molecular structures. Its fluorinated and amino functional groups enable selective reactions and facilitate the introduction of fluorine atoms into organic frameworks, a feature highly sought after in medicinal chemistry and material science. By utilizing this compound as a starting material, chemists can access a wide range of fluorine-containing compounds with diverse applications.Moreover, the presence of both the fluoro and trifluoromethyl moieties in 3-Fluoro-4-(trifluoromethyl)pyridin-2-amine enhances the lipophilicity and electron-withdrawing effects of the molecules it is incorporated into, making it an ideal candidate for designing bioactive molecules with optimized properties. Its compatibility with various synthetic methodologies further expands the scope of its applications in chemical synthesis, enabling the efficient preparation of novel compounds with potential therapeutic or industrial significance.
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