CAS 4593-16-2
:1-(3-Methyl-1-piperidinyl)ethanone
Description:
1-(3-Methyl-1-piperidinyl)ethanone, also known by its CAS number 4593-16-2, is an organic compound characterized by its piperidine ring structure, which contributes to its basicity and potential for forming hydrogen bonds. This compound features a ketone functional group, which is indicative of its reactivity and ability to participate in various chemical reactions, such as nucleophilic additions. The presence of the methyl group on the piperidine ring enhances its steric properties and can influence its interaction with biological systems. Typically, compounds like this may exhibit psychoactive properties, making them of interest in pharmacological research. Its solubility in organic solvents and moderate polarity can facilitate its use in synthetic applications and as an intermediate in organic synthesis. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity. Overall, 1-(3-Methyl-1-piperidinyl)ethanone is a compound of interest in both synthetic organic chemistry and medicinal chemistry.
Formula:C8H15NO
InChI:InChI=1S/C8H15NO/c1-7-4-3-5-9(6-7)8(2)10/h7H,3-6H2,1-2H3
InChI key:InChIKey=XKFPNHDGLSYZRC-UHFFFAOYSA-N
SMILES:C(C)(=O)N1CC(C)CCC1
Synonyms:- 1-(3-Methyl-1-piperidinyl)ethanone
- 1-(3-Methylpiperidin-1-Yl)Ethanone
- 1-(3-Methylpiperidin-1-yl)ethan-1-one
- 3-Pipecoline, 1-acetyl-
- Ethanone, 1-(3-methyl-1-piperidinyl)-
- Piperidine, 1-acetyl-3-methyl-
- 1-Acetyl-3-methylpiperidine
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1-Acetyl-3-methylpiperidine
CAS:Formula:C8H15NOColor and Shape:Liquid, No data available.Molecular weight:141.214
