CAS 25519-79-3

1-(4-Benzoyl-1-piperidinyl)ethanone

Description:

1-(4-Benzoyl-1-piperidinyl)ethanone, also known by its CAS number 25519-79-3, is an organic compound characterized by its piperidine ring structure substituted with a benzoyl group and an ethanone moiety. This compound typically appears as a solid or crystalline substance and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its molecular structure includes a piperidine ring, which contributes to its basicity and potential interactions with biological targets. The presence of the benzoyl group enhances its lipophilicity, which can influence its absorption and distribution in biological systems. Additionally, the ethanone functional group may participate in various chemical reactions, making this compound a versatile intermediate in organic synthesis. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken. Overall, 1-(4-Benzoyl-1-piperidinyl)ethanone is of interest for its structural features and potential utility in chemical research and drug development.

Formula: C₁₄H₁₇NO₂

InChI: InChI=1S/C14H17NO2/c1-11(16)15-9-7-13(8-10-15)14(17)12-5-3-2-4-6-12/h2-6,13H,7-10H2,1H3

InChI key: InChIKey=RQVMJPJBWMFWFT-UHFFFAOYSA-N

SMILES: C(=O)(C1CCN(C(C)=O)CC1)C2=CC=CC=C2

Synonyms:

• 1-(4-Benzoylpiperidin-1-yl)ethanone
• 1-(4-Benzoyl-1-piperidinyl)ethanone
• 1-Acetyl-4-benzoylpiperidine
• Piperidine, 1-acetyl-4-benzoyl-
• Ethanone, 1-(4-benzoyl-1-piperidinyl)-

1-Acetyl-4-benzoylpiperidine

Controlled Product

CAS: 25519-79-3

Applications A synthetic intermediate in the preparation of CNS depressants.
References Duncan, R.L. Jr., et al.: J. Med. Chem., 13, 1, 1 (1970); Walsh, D., et al.: J. Med. Chem., 32, 105 (1989), Katritzky, A., et al.: Proc. Natl. Acad. Sci. USA., 105, 7359 (2008),

Formula: C₁₄H₁₇NO₂

Color and Shape: Neat

Molecular weight: 231.29

Ref: TR-A170625