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N-Ethylpiperidinone

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Identification
Molecular formula
C7H13NO
CAS number
766-09-6
IUPAC name
1-(1-piperidyl)ethanone
State
State

At room temperature, N-Ethylpiperidinone is a liquid. Its state can be affected by ambient temperature, but it remains stable and fluid under normal conditions.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
113.17g/mol
Molar mass
113.1730g/mol
Density
1.0320g/cm3
Appearence

N-Ethylpiperidinone appears as a colorless to pale yellow liquid. It is highly soluble in water and has a slightly pungent odor.

Comment on solubility

Solubility of 1-(1-piperidyl)ethanone

1-(1-piperidyl)ethanone, a compound characterized by its unique structure, exhibits interesting solubility properties that are noteworthy in various contexts.

Solubility Characteristics

In general, the solubility of 1-(1-piperidyl)ethanone can be summarized as follows:

  • Water Solubility: This compound is moderately soluble in water, attributed to its polar functional groups that can interact with water molecules.
  • Organic Solvents: It shows good solubility in a variety of organic solvents such as ethanol, methanol, and acetone, which allows it to be utilized effectively in organic synthesis and pharmaceutical formulations.
  • Temperature Dependence: Its solubility can vary with temperature, often increasing with heating, which is a common behavior for many organic compounds.

This versatility in solubility not only facilitates its use in laboratory settings but also influences its application in medicinal chemistry and pharmaceutical development. As with many chemicals, testing solubility in specific solvents is vital to ensure optimal performance in reactions and formulations.

Interesting facts

Interesting Facts about 1-(1-Piperidyl)ethanone

1-(1-Piperidyl)ethanone, also known as 1-piperidinoacetone, is a fascinating compound that finds application in various chemical and pharmaceutical areas.

Key Features

  • Structure and Functionality: The compound features a piperidine ring, which is a saturated six-membered ring containing one nitrogen atom. This structure is known for its ability to act as a versatile building block in organic synthesis.
  • Pharmaceutical Relevance: 1-(1-Piperidyl)ethanone is often investigated for pharmacological activity. Compounds with piperidine moieties are frequently found in drugs targeting central nervous system disorders.
  • Synthesis: The synthesis of this compound usually involves straightforward methods that highlight the utility of piperidine in crafting new chemical entities.

Fun Facts

  • The piperidine ring is historically significant in medicinal chemistry, serving as a core structure for various important pharmaceuticals.
  • Researchers value the compound for its potential to develop novel therapeutic agents through modification of its chemical structure.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This sentiment resonates within the field of organic chemistry, particularly in exploring derivatives of compounds like 1-(1-piperidyl)ethanone for innovative applications.

Overall, 1-(1-piperidyl)ethanone exemplifies the intersection of organic chemistry and medicinal applications, showcasing how a simple compound can lead to significant advancements in science.

Synonyms
1-ACETYLPIPERIDINE
618-42-8
Piperidine, 1-acetyl-
1-(piperidin-1-yl)ethan-1-one
Ethanone, 1-(1-piperidinyl)-
NSC 239
1-(1-piperidinyl)ethanone
EINECS 210-550-5
BRN 0109570
CHEBI:36591
AI3-11533
DTXSID7060679
5-20-02-00440 (Beilstein Handbook Reference)
DTXCID5043130
inchi=1/c7h13no/c1-7(9)8-5-3-2-4-6-8/h2-6h2,1h
kdismimtgumord-uhfffaoysa-n
1-(Piperidin-1-yl)ethanone
N-Acetylpiperidine
N-Acetylpiperidin
Acetic acid, piperidide
N-Acetyl piperidine
Methyl 1-piperidyl ketone
1-piperidin-1-ylethanone
1-Piperidin-1-yl-ethanone
MFCD00006486
6YC8YEW5QR
NSC-239
N-Acetylpiperidin [German]
UNII-6YC8YEW5QR
1-(1-piperidyl)ethanone
SCHEMBL8053
CHEMBL12196
NSC239
AKOS003846742
AC-2947
AS-58709
SY106654
DB-054003
A0109
CS-0155037
NS00034811
S12042
Q27116893
F0808-1080