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Fenobucarb

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Identification
Molecular formula
C12H17NO3
CAS number
3766-81-2
IUPAC name
[3-(but-2-enoylamino)phenyl] N-isopropylcarbamate
State
State

Fenobucarb is typically found as a liquid or solid under ambient conditions, depending on its specific formulation and purity.

Melting point (Celsius)
29.00
Melting point (Kelvin)
302.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
221.27g/mol
Molar mass
221.2690g/mol
Density
1.1000g/cm3
Appearence

Fenobucarb appears as a brown liquid or crystalline solid. It has a characteristic aromatic odor typical of carbamate compounds.

Comment on solubility

Solubility of [3-(but-2-enoylamino)phenyl] N-isopropylcarbamate

The solubility of [3-(but-2-enoylamino)phenyl] N-isopropylcarbamate can be quite intriguing and depends on several factors, including the compound's chemical structure and the environment in which it is assessed.

  • Polarity: The presence of functional groups such as amino and carbamate can influence polarity, affecting how well the compound dissolves in various solvents.
  • Solvent Compatibility: It is likely to be more soluble in polar solvents like methanol or water due to the potential for hydrogen bonding, while showing limited solubility in non-polar solvents.
  • Temperature Dependence: As with many organic compounds, increasing the temperature often enhances solubility, suggesting that higher temperatures could facilitate the dissolution process.
  • pH Influence: For compounds containing basic or acidic functional groups, changes in pH can significantly alter solubility, making it important to consider the acidity or basicity of the solution.

In summary, the solubility of [3-(but-2-enoylamino)phenyl] N-isopropylcarbamate is governed by a complex interplay of its chemical characteristics and the nature of the solvent. As one researcher aptly put it, “Understanding the solubility of a compound is key to harnessing its full potential in applications.” Thus, careful evaluation of its solubility profile under different conditions is critical for practical uses.

Interesting facts

Exploring [3-(but-2-enoylamino)phenyl] N-isopropylcarbamate

[3-(but-2-enoylamino)phenyl] N-isopropylcarbamate is a fascinating compound known for its unique chemical structure and potential applications in the fields of pharmaceuticals and biochemistry. As a derivative of carbamic acid, it participates in various biological processes, making it quite significant in research.

Key Features

  • Amide Bond: The compound contains an amide functional group that is crucial in the formation of peptide bonds, highlighting its importance in protein structure.
  • Unsaturated Moiety: The presence of a but-2-enoyl group introduces unsaturation, which can influence reactivity and interaction with biological systems.
  • Substituted Aromatic Ring: The phenyl group in the structure contributes to the hydrophobic character and electronic properties that can modulate biological activity.

This compound is not only an interesting molecular entity but also acts as a probe for studying various chemical reactions and mechanisms. The combination of its functional groups allows scientists to explore potential therapeutic activities, such as:

  • Antimicrobial properties
  • Anticancer activity
  • Enzyme inhibitors

With ongoing research, [3-(but-2-enoylamino)phenyl] N-isopropylcarbamate exemplifies the marriage of organic chemistry and medicinal applications, showcasing how intricate molecular design can pave the way for innovative solutions in health and science. As one chemist aptly said, "The beauty of chemistry lies in the endless possibilities of how simple molecules can lead to complex biological interactions."

Synonyms
NSC-222513
[3-(But-2-enoylamino)phenyl]n-propan-2-ylcarbamate
L3A93DR6SC
orb1986244
N-Isopropylcarbamic acid 3-[(1-oxo-2-butenyl)amino]phenyl ester
Carbamic acid, (1-methylethyl)-, 3-[(1-oxo-2-butenyl)amino]phenyl ester