AA55810
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 96% | in stock | $219.00 | $153.00 | - + | |
1g | 96% | in stock | $558.00 | $391.00 | - + | |
5g | 96% | in stock | $2,190.00 | $1,533.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA55810 |
Chemical Name: | Methyl 5-fluoro-2-methoxypyridine-3-carboxylate |
CAS Number: | 122433-52-7 |
Molecular Formula: | C8H8FNO3 |
Molecular Weight: | 185.1524 |
MDL Number: | MFCD14698160 |
SMILES: | COC(=O)c1cc(F)cnc1OC |
Complexity: | 188 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 5 |
Rotatable Bond Count: | 3 |
XLogP3: | 1.1 |
Methyl 5-fluoro-2-methoxynicotinate is a valuable compound that finds significant application in chemical synthesis processes. This compound serves as a versatile building block in organic chemistry, particularly in the development of pharmaceuticals, agrochemicals, and materials science. Its unique structure and functional groups make it an essential intermediate for the synthesis of various biologically active compounds.In chemical synthesis, Methyl 5-fluoro-2-methoxynicotinate can participate in various reactions such as esterification, nucleophilic substitution, or coupling reactions. Its fluoro and methoxy substituents confer specific properties to the molecule, allowing for the creation of diverse chemical entities with tailored functionalities. Additionally, the presence of the nicotinic acid scaffold in this compound offers opportunities for further derivatization to access novel molecules with enhanced biological activities.Researchers and synthetic chemists often utilize Methyl 5-fluoro-2-methoxynicotinate as a key starting material to introduce fluorine and methoxy groups into target molecules. These substitutions can significantly influence the physicochemical and pharmacological properties of the final compounds, making them more potent or selective in their biological activities. By incorporating this compound into their synthetic routes, chemists can streamline the synthesis of complex molecules and expedite the drug discovery process.Overall, Methyl 5-fluoro-2-methoxynicotinate plays a crucial role in advancing the field of chemical synthesis by enabling the efficient construction of structurally diverse and biologically relevant molecules. Its strategic use in designing new materials and pharmaceutical agents underscores its importance as a building block in organic chemistry research and development.