2-Piperidineacetic acid, ethyl ester, with the CAS number 2739-99-3, is an organic compound characterized by its piperidine ring structure, which is a six-membered ring containing one nitrogen atom. This compound features an acetic acid moiety, where the carboxylic acid group is esterified with an ethyl group, enhancing its solubility in organic solvents. It typically appears as a colorless to pale yellow liquid and has a moderate boiling point. The presence of the piperidine ring contributes to its basicity and potential for forming hydrogen bonds, which can influence its reactivity and interactions with biological systems. This compound is often utilized in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its safety profile should be considered, as it may exhibit irritant properties. Proper handling and storage conditions are essential to ensure safety and stability.

2-Piperidineacetic acid, ethyl ester

2739-99-3: (±)-Ethyl 2-piperidineacetate, 2-Piperidineacetic acid, ethyl ester, Ethyl 2-piperidinylacetate,  Ethyl piperidin-2-ylacetate

Ethyl piperidin-2-ylacetate is a stereoisomer of piperidine, which has the molecular formula CH3CH2CH2CH2C6H5COCH3. It is a condensation product of ethyl acetate and ammonia. Ethyl piperidin-2-ylacetate is an efficient method for the synthesis of lactams. This isomer can be used to produce amides and catalytic reduction products.

CAS 2739-99-3: 2-Piperidineacetic acid, ethyl ester

Ethyl piperidin-2-ylacetate

Ref: 3D-CAA73999

Ethyl piperidin-2-ylacetate

Ref: 54-OR953444

ETHYL 2-PIPERIDINEACETATE

Ref: IN-DA003Q1I

Ethyl piperidin-2-ylacetate

Ref: 10-F330474