AA10614
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $122.00 | $86.00 | - + | |
250mg | 98% | in stock | $179.00 | $125.00 | - + | |
1g | 98% | in stock | $542.00 | $380.00 | - + | |
5g | 98% | in stock | $1,536.00 | $1,075.00 | - + | |
10g | 98% | in stock | $2,625.00 | $1,837.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA10614 |
Chemical Name: | (R)-5-Hydroxypiperidin-2-one |
CAS Number: | 102774-92-5 |
Molecular Formula: | C5H9NO2 |
Molecular Weight: | 115.1305 |
MDL Number: | MFCD06202375 |
SMILES: | O[C@@H]1CCC(=O)NC1 |
Complexity: | 103 |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Heavy Atom Count: | 8 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
XLogP3: | -1 |
The chiral compound (R)-5-Hydroxy-2-piperidinone, also known as 1-((R)-hydroxy(4-oxo-2-piperidinyl))-ethanone, is a valuable building block in chemical synthesis due to its versatile reactivity and unique stereochemistry. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, (R)-5-Hydroxy-2-piperidinone can be utilized as a chiral ligand for asymmetric catalysis, enabling the enantioselective synthesis of complex molecules. Its hydroxyl and piperidinone functional groups also make it a valuable precursor for the construction of heterocyclic compounds through cyclization reactions.Furthermore, the presence of the hydroxyl group in (R)-5-Hydroxy-2-piperidinone allows for facile derivatization, enabling the introduction of additional functional groups to tailor the molecule's properties for specific synthetic pathways. Its stereochemistry is crucial in controlling the stereochemical outcome of reactions, leading to the formation of enantiomerically pure products.Overall, (R)-5-Hydroxy-2-piperidinone plays a crucial role in chemical synthesis by providing a versatile and enantioselective building block for the construction of diverse molecular architectures with high stereochemical control.