AB64986
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $12.00 | $9.00 | - + | |
1g | 98% | in stock | $32.00 | $22.00 | - + | |
5g | >95% | in stock | $113.00 | $79.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB64986 |
Chemical Name: | 3-Fluoro-4-piperidinone, HCl |
CAS Number: | 1070896-59-1 |
Molecular Formula: | C5H9ClFNO |
Molecular Weight: | 153.5825 |
MDL Number: | MFCD11506659 |
SMILES: | O=C1CCNCC1F.Cl |
Complexity: | 105 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Undefined Atom Stereocenter Count: | 1 |
3-Fluoro-4-piperidone Hydrochloride is a versatile compound that finds extensive application in chemical synthesis, particularly in the pharmaceutical industry. Due to its unique structure and properties, this compound serves as a valuable building block for the development of various organic molecules and drug candidates. One key application of 3-Fluoro-4-piperidone Hydrochloride is its role as a precursor in the synthesis of fluorinated compounds. The fluorine atom present in the structure imparts distinct characteristics and can modulate the physicochemical properties of the final product. This compound can be used in the synthesis of fluorinated pharmaceuticals, agrochemicals, and materials with enhanced properties.Furthermore, 3-Fluoro-4-piperidone Hydrochloride can participate in diverse chemical reactions, such as nucleophilic substitution, acylation, and cyclization processes. Its combination of the piperidone ring and fluorine substitution offers opportunities for selective functionalization and structural modifications, allowing for the creation of structurally complex molecules with specific biological activities.Overall, the application of 3-Fluoro-4-piperidone Hydrochloride in chemical synthesis enables the efficient and strategic construction of molecular scaffolds with desired properties, making it a valuable tool in the design and development of novel compounds for various applications.