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AE64116

1214344-68-9 | 2-Fluoro-5-(trifluoromethyl)pyrimidine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $105.00 $74.00 -   +
1g 98% in stock $241.00 $169.00 -   +
5g 98% in stock $898.00 $629.00 -   +
10g 98% in stock $1,535.00 $1,074.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE64116
Chemical Name: 2-Fluoro-5-(trifluoromethyl)pyrimidine
CAS Number: 1214344-68-9
Molecular Formula: C5H2F4N2
Molecular Weight: 166.0764
MDL Number: MFCD13185662
SMILES: Fc1ncc(cn1)C(F)(F)F

 

Computed Properties
Complexity: 127  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 6  
XLogP3: 1.5  

 

 

Upstream Synthesis Route
  • 2-Fluoro-5-(trifluoromethyl)pyrimidine, also known as $name$, is a versatile compound widely utilized in chemical synthesis. With its unique structural properties, this compound plays a crucial role in various organic reactions and transformations.In the realm of chemical synthesis, 2-fluoro-5-(trifluoromethyl)pyrimidine serves as a valuable building block for the creation of complex organic molecules. Its fluorine and trifluoromethyl groups confer distinctive reactivity and can be harnessed for diverse functionalization strategies.One key application of 2-fluoro-5-(trifluoromethyl)pyrimidine is in the synthesis of pharmaceuticals and agrochemicals. The presence of the fluorine atom enhances the biological activity of the resulting compounds, making it an attractive choice for medicinal chemistry projects. Additionally, the trifluoromethyl group provides steric hindrance and lipophilicity that can influence the physicochemical properties of the target molecules.Furthermore, this compound can participate in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, enabling the construction of carbon-carbon and carbon-nitrogen bonds. Its use in various transformations, such as halogenation, arylation, and alkylation, showcases its utility as a versatile synthetic building block.Overall, the application of 2-fluoro-5-(trifluoromethyl)pyrimidine in chemical synthesis underscores its importance as a valuable tool for the development of novel compounds with diverse functionalities and applications in the fields of pharmaceuticals, materials science, and beyond.
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