CAS 50675-20-2
:4-Piperidinecarboxaldehyde
Description:
4-Piperidinecarboxaldehyde, with the CAS number 50675-20-2, is an organic compound characterized by a piperidine ring substituted with an aldehyde group at the 4-position. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in polar organic solvents and exhibits moderate stability under standard conditions. The presence of the aldehyde functional group makes it reactive, particularly in condensation reactions and as a potential electrophile in various organic syntheses. 4-Piperidinecarboxaldehyde is often utilized in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its ability to serve as an intermediate in the formation of more complex molecules. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential, as with many aldehydes, to avoid polymerization and ensure safety due to potential irritant properties.
Formula:C6H11NO
InChI:InChI=1S/C6H11NO/c8-5-6-1-3-7-4-2-6/h5-7H,1-4H2
InChI key:InChIKey=HRVXPXCISZSDCC-UHFFFAOYSA-N
SMILES:C(=O)C1CCNCC1
Synonyms:- 4-Formylpiperidine
- 4-Piperidinecarboxaldehyde
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Found 3 products.
Piperidine-4-carboxaldehyde
CAS:<p>Piperidine-4-carboxaldehyde</p>Formula:C6H11NOPurity:95%Color and Shape: beige crystalline solidMolecular weight:113.16g/molPiperidine-4-carbaldehyde
CAS:<p>Piperidine-4-carbaldehyde (Piperidine-4-carboxaldehyde) serves as a PROTAC linker. It is employed to enhance the binding affinity to target proteins, thereby increasing the degradation efficiency of PROTAC molecules. Additionally, Piperidine-4-carbaldehyde is utilized in the synthesis of CDK2 PROTACs.</p>Formula:C6H11NOMolecular weight:113.16



