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2-isopropylpent-4-enamide

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Identification
Molecular formula
C8H15NO
CAS number
101811-75-8
IUPAC name
2-isopropylpent-4-enamide
State
State
The compound is typically found in a liquid state at room temperature, making it suitable for various chemical synthesis applications.
Melting point (Celsius)
-45.50
Melting point (Kelvin)
227.65
Boiling point (Celsius)
218.50
Boiling point (Kelvin)
491.65
General information
Molecular weight
127.20g/mol
Molar mass
127.2020g/mol
Density
0.9005g/cm3
Appearence

2-isopropylpent-4-enamide appears as a colorless to light yellow liquid, with a characteristic faint amine odor. The compound is typically clear, though impurities can lead to slight cloudiness or coloration.

Comment on solubility

Solubility of 2-isopropylpent-4-enamide

2-isopropylpent-4-enamide, a compound with the molecular structure C8H15NO, showcases intriguing solubility characteristics driven by its molecular design.

  • Polarity: The presence of an amide functional group contributes to the compound's polarity, which can enhance solubility in polar solvents.
  • Solvent Influence: It is generally soluble in common polar organic solvents like methanol and ethanol due to hydrogen bonding capabilities.
  • Hydrophobic Interaction: Conversely, the isopropyl group introduces hydrophobic characteristics, which can limit solubility in strictly non-polar solvents such as hexane.
  • Temperature Factors: As with many organic compounds, solubility may increase with temperature, allowing for a better dissolution in chosen solvents.

Overall, the solubility of 2-isopropylpent-4-enamide illustrates a complex interplay between its hydrophilic amide group and its hydrophobic hydrocarbon chains, making it soluble in polar environments while presenting challenges in non-polar media.

Interesting facts

Interesting Facts About 2-isopropylpent-4-enamide

2-isopropylpent-4-enamide, also known in some contexts as an important chemical intermediate, is characterized by its unique structure and various applications in the field of organic chemistry.

Key Characteristics:

  • Structure: This compound features a long carbon chain with functional groups that lead to interesting reactivity, making it a significant building block in organic synthesis.
  • Applications: 2-isopropylpent-4-enamide is often utilized in the production of pharmaceuticals, where it serves as an intermediate in synthesizing active pharmaceutical ingredients (APIs).
  • Reactivity: The presence of the amide functional group allows for a variety of chemical reactions, including nucleophilic attack and condensation reactions.
  • Natural Occurrence: Compounds related to this structure can sometimes be found in natural products, leading to potential applications in biochemistry and pharmacology.

Chemical Insights:

From a scientific perspective, studying 2-isopropylpent-4-enamide can enhance our understanding of:

  • Reaction Mechanisms: Investigating how this compound behaves under different conditions can illustrate fundamental concepts within organic reaction mechanisms.
  • Structure-Activity Relationships: Understanding how the structure influences the activity of the compound can further its applicability in drug design and development.
  • Intermolecular Interactions: The characteristics of amides in this compound highlight the significance of hydrogen bonding and other intermolecular forces in influencing physical and chemical properties.

Overall, 2-isopropylpent-4-enamide represents a fascinating intersection of organic chemistry and applied science, showcasing the continuous need for exploration and innovation in the field.

Synonyms
ALLYLISOPROPYLACETAMIDE
299-78-5
2-isopropylpent-4-enamide
2-Isopropyl-4-Pentenamide
2-propan-2-ylpent-4-enamide
4-Pentenamide, 2-(1-methylethyl)-
4-Pentenamide,2-(1-methylethyl)-
ZOF4719QS5
AI3-61022
UNII-ZOF4719QS5
2-allyl-2-isopropylacetamide
2 Isopropyl 4 Pentenamide
SCHEMBL3322985
DTXSID20952350
HINLFAQOKAHXOD-UHFFFAOYSA-N
2-(1-Methylethyl)-4-pentenamide
AKOS006278029
2-(Propan-2-yl)pent-4-enimidic acid
Ro 01-0973
WS-01610
W18852
Q27295821