CAS 24686-78-0

1-Benzoyl-4-piperidone

Description:

1-Benzoyl-4-piperidone, with the CAS number 24686-78-0, is an organic compound that belongs to the class of piperidones. It features a piperidine ring substituted at the 4-position with a benzoyl group, which contributes to its distinctive chemical properties. This compound typically appears as a solid or crystalline substance and is known for its potential applications in organic synthesis and medicinal chemistry. It exhibits characteristics such as moderate solubility in organic solvents and limited solubility in water, which is common for many piperidone derivatives. The presence of the carbonyl group in the benzoyl moiety allows for reactivity in various chemical reactions, including nucleophilic additions and condensation reactions. Additionally, 1-benzoyl-4-piperidone may exhibit biological activity, making it of interest in pharmaceutical research. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper laboratory practices are followed.

Formula: C₁₂H₁₃NO₂

InChI: InChI=1S/C12H13NO2/c14-11-6-8-13(9-7-11)12(15)10-4-2-1-3-5-10/h1-5H,6-9H2

InChI key: InChIKey=NZAXGZYPZGEVBD-UHFFFAOYSA-N

SMILES: C(=O)(N1CCC(=O)CC1)C2=CC=CC=C2

Synonyms:

• 1-Benzoyl-4-oxopiperidine
• 1-Benzoyl-4-piperidinone
• 1-Benzoyl-4-piperidone
• 1-Benzoylpiperidin-4-One
• 4-Piperidinone, 1-benzoyl-
• 4-Piperidone, 1-benzoyl-
• NSC 97564
• N-Benzoyl-4-piperidone

1-Benzoyl-4-piperidone

CAS: 24686-78-0

Formula: C₁₂H₁₃NO₂

Purity: >97.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 203.24

Ref: 3B-B3778

N-Benzoyl-4-piperidone

CAS: 24686-78-0

Formula: C₁₂H₁₃NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 203.2371

Ref: IN-DA00BBPP

N-Benzoyl-4-piperidone

CAS: 24686-78-0

Formula: C₁₂H₁₃NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 203.241

Ref: 10-F036875

N-Benzoylpiperidone

Controlled Product

CAS: 24686-78-0

N-Benzoylpiperidone is a synthetic piperidine derivative that is used in the synthesis of other organic compounds. It can be synthesized by reacting phenylacetaldehyde with chloroacetonitrile and hydroxybenzene. It can also be synthesized by reacting bromoacetonitrile with hydroxybenzene in the presence of sodium hydroxide. The compound has two stereoisomers, which are determined by the configuration at the nitrogen atom. The N-benzoyl group on one stereoisomer binds to the intramolecular hydrogen molecule, which signifies its structural analysis. These two isomers are distinguished by their hydroxy group, amide and alkylation properties. They react differently with rat liver microsomes due to different substrate concentration.

Formula: C₁₂H₁₃NO₂

Purity: (%) Min. 95%

Color and Shape: Powder

Molecular weight: 203.23 g/mol

Ref: 3D-FB142667

1-Benzoylpiperidin-4-one

CAS: 24686-78-0

1-Benzoylpiperidin-4-one

Purity: 98%

Color and Shape: Off-White Powder

Molecular weight: 203.24g/mol

Ref: 54-OR9378