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N-Ethylacetoacetamide

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Identification
Molecular formula
C6H11NO2
CAS number
1118-62-1
IUPAC name
N-ethyl-3-oxo-butanamide
State
State

N-Ethylacetoacetamide is typically a liquid at room temperature. It flows freely and exhibits typical liquid behavior, such as adapting to the shape of its container.

Melting point (Celsius)
-37.00
Melting point (Kelvin)
236.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
143.17g/mol
Molar mass
143.1730g/mol
Density
0.9955g/cm3
Appearence

N-Ethylacetoacetamide is a colorless to pale yellow liquid. It has a slight amine odor. Its consistency and appearance could be likened to that of a light oil, making it distinct in texture compared to solid chemical compounds.

Comment on solubility

Solubility of N-ethyl-3-oxo-butanamide (C6H11NO2)

N-ethyl-3-oxo-butanamide is a compound whose solubility properties are quite interesting due to its molecular structure and functional groups. The solubility of this compound can be attributed to several factors:

  • Polarity: The presence of the amide group contributes to polar characteristics, making it more soluble in polar solvents, particularly water.
  • Hydrogen Bonding: The ability of N-ethyl-3-oxo-butanamide to form hydrogen bonds enhances its solubility in aqueous solutions.
  • Organic Solvents: It tends to dissolve well in organic solvents like ethanol and acetone due to the compatibility with non-polar regions of the organic solvent molecules.

However, it's important to note that solubility may be affected by temperature and concentration. In general, compounds like N-ethyl-3-oxo-butanamide can offer some solubility challenges or advantages:

  1. Increased temperature: Usually leads to higher solubility in most solvents.
  2. Concentration effects: At higher concentrations, solubility can decrease due to saturation limits.

In conclusion, understanding the solubility of N-ethyl-3-oxo-butanamide can provide insights into its behavior in various chemical environments, showcasing its relevance in both organic synthesis and potential applications in various fields.

Interesting facts

Exploring N-ethyl-3-oxo-butanamide

N-ethyl-3-oxo-butanamide is a fascinating compound that plays a significant role in various chemical reactions and applications. Here are some interesting facts about this compound:

  • Functional Groups: N-ethyl-3-oxo-butanamide contains both an amide and a ketone functional group. This dual composition makes it an interesting target for myriad chemical transformations.
  • Versatile Reactions: Its structure allows it to participate in numerous reactions, including Michael additions and amide bond formation, which are crucial in synthetic organic chemistry.
  • Biological Relevance: Compounds like N-ethyl-3-oxo-butanamide often serve as precursors or intermediates in the synthesis of bioactive molecules, which can lead to important pharmaceutical agents.
  • Synthesis Methods: Chemists can synthesize this compound through various methods, including condensation reactions. Understanding these methods can enhance a student's appreciation of organic synthesis.
  • Research Potential: Due to its unique properties, there may be unexplored applications for N-ethyl-3-oxo-butanamide in materials science or medicinal chemistry. Ongoing research may yield novel insights.

In conclusion, N-ethyl-3-oxo-butanamide is not just a simple compound; it embodies the complexity and versatility of organic chemistry. The interplay of its functional groups opens several pathways for researchers and students alike, making it a compelling subject of study.

Synonyms
N-Ethyl-3-oxobutanamide
N-Ethyl acetoacetamide
N-ethylacetoacetamide
Butanamide, N-ethyl-3-oxo-
ACETOACETAMIDE, N-ETHYL-
BRN 1754233
UNII-GN725IYQ3Q
Ethylamid kyseliny acetoctove
GN725IYQ3Q
Ethylamid kyseliny acetoctove [Czech]
DTXSID7040108
DTXCID5020108
Butanamide, N-ethyl-3-oxo-(9CI)
4-04-00-00409 (beilstein handbook reference)
10138-46-2
Ethyl acetoacetalamide
SCHEMBL649664
SCHEMBL1417216
SCHEMBL1417217
REYAJCIAOQNQTF-UHFFFAOYSA-N
AKOS000165670
DB-321140
Q27279185