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N-Ethylbenzamide

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Identification
Molecular formula
C9H11NO
CAS number
93-89-0
IUPAC name
N-ethylbenzamide
State
State

At room temperature, N-Ethylbenzamide is in a solid state. It is typically characterized by its crystalline form.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
301.00
Boiling point (Kelvin)
574.15
General information
Molecular weight
149.19g/mol
Molar mass
149.1890g/mol
Density
1.0440g/cm3
Appearence

N-Ethylbenzamide is a white to off-white crystalline solid. It may also be found as a powder depending on the specific sample preparation and conditions.

Comment on solubility

Solubility of N-ethylbenzamide

N-ethylbenzamide, a member of the amide class, displays interesting solubility characteristics. Understanding its solubility is crucial for various applications in both laboratory and industrial settings.

Solubility Insights

  • Solvent Polarity: N-ethylbenzamide is relatively soluble in polar solvents such as water and ethanol, but exhibits better solubility in non-polar solvents like ether and chloroform.
  • Temperature Influence: Like many organic compounds, the solubility of N-ethylbenzamide can increase with temperature, allowing for greater dissolution in solvent when heated.
  • pH Considerations: The solubility can also be affected by the pH of the solution, particularly due to the amide functional group’s behavior in acidic or basic conditions.

As a general guideline, "the greater the polarity of the solvent, the better the solubility of organic polar compounds,” and N-ethylbenzamide falls within this rule, showcasing moderate to good solubility in suitable solvents. Overall, understanding its solubility profile can greatly enhance its utilization across different chemical processes.

Interesting facts

Interesting Facts about N-ethylbenzamide

N-ethylbenzamide is a fascinating compound with unique properties and applications that make it notable in the field of chemistry. This amide derivative showcases the versatility of carbon-containing compounds and highlights the significance of functional groups in organic chemistry.

Key Points to Consider:

  • Chemical Structure: N-ethylbenzamide features an ethyl group attached to the nitrogen atom of an amide formed from benzoic acid. This structural characteristic influences its behavior and interactions in chemical reactions.
  • Applications: This compound is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its role in drug development showcases how small changes in molecular structure can lead to significant biological effects.
  • Research Interest: Scientists study N-ethylbenzamide for its potential applications in medicinal chemistry. The understanding of its reactivity and substitution patterns provides insights for developing new compounds with desired properties.
  • Physical properties: The presence of an ethyl group contributes to its molecular interactions, affecting solubility and reactivity with other compounds, which are essential factors in organic synthesis.

"The beauty of chemistry lies in the small details." This sentiment resonates with the study of compounds like N-ethylbenzamide, where each modification can lead to a new understanding or application. By investigating N-ethylbenzamide, chemists can delve deeper into the world of amides and their significance in both synthesis and application.

In conclusion, N-ethylbenzamide is not just another compound; it represents the rich tapestry of organic chemistry, inviting exploration and discovery.

Synonyms
N-Ethylbenzamide
614-17-5
BENZAMIDE, N-ETHYL-
NSC 20558
BRN 2043576
SW509B0V2A
AI3-01070
NSC-20558
DTXSID10210315
DTXCID10132806
664-988-0
N-ethyl-benzamide
NSC20558
N-Ethyl-benzamide (10)
WLN: 2MVR
UNII-SW509B0V2A
SCHEMBL162323
CHEMBL500597
BDBM233171
MFCD00026702
AKOS003235698
DB-053875
EN300-6772057