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latestatin

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Identification
Molecular formula
C12H16N2O3
CAS number
97488-09-0
IUPAC name
1-carbamoyl-3-[2-(4-methoxyphenyl)ethyl]urea
State
State

This compound is typically a solid at room temperature. It is stable under standard conditions.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
252.27g/mol
Molar mass
252.2820g/mol
Density
1.2420g/cm3
Appearence

Latestatin appears as a white crystalline powder. It is typically homogeneous and fine in texture.

Comment on solubility

Solubility of 1-Carbamoyl-3-[2-(4-methoxyphenyl)ethyl]urea

The solubility of 1-carbamoyl-3-[2-(4-methoxyphenyl)ethyl]urea can be influenced by various factors, including temperature, pH, and the nature of the solvent. Typically, compounds containing urea functional groups are known for their moderate solubility in polar solvents.

Factors Affecting Solubility:

  • Temperature: An increase in temperature often enhances solubility for many organic compounds, including ureas.
  • Solvent Polarity: 1-carbamoyl-3-[2-(4-methoxyphenyl)ethyl]urea is likely to be more soluble in polar protic solvents like water or alcohols due to hydrogen bonding capabilities.
  • pH Levels: Variations in pH may affect the ionization state of the urea moiety, which can further influence solubility characteristics.

In summary, while 1-carbamoyl-3-[2-(4-methoxyphenyl)ethyl]urea is expected to demonstrate adequate solubility in polar solvents, precise solubility data can only be determined under specific experimental conditions. As with many organic compounds, understanding the interplay between structural features and solvent characteristics is key to predicting solubility behavior.

Interesting facts

Interesting Facts about 1-Carbamoyl-3-[2-(4-methoxyphenyl)ethyl]urea

1-Carbamoyl-3-[2-(4-methoxyphenyl)ethyl]urea is a fascinating compound that highlights the intriguing intersection of urea derivatives and aromatic chemistry. This compound, structured with both carbamoyl and ethyl groups, showcases significant potential in various fields of study.

Chemical Significance

  • Reactivity: The presence of the carbamoyl group makes this compound a remarkable candidate for studies involving nitrogen-containing frameworks, which are essential in medicinal chemistry.
  • Biological Relevance: Compounds with similar structures have shown promising biological activities, particularly in pharmaceutical applications where they can act as enzyme inhibitors or targeted therapeutic agents.
  • Aromatic Influence: The incorporation of a 4-methoxyphenyl group not only enhances the compound's structural complexity but also influences its lipophilicity and interaction with biological targets.

Applications and Research

This compound is currently a topic of interest due to its potential applications in:

  • Drug Development: As researchers seek new drugs, compounds like this one may provide skeletons for creating novel therapeutic agents.
  • Agricultural Chemistry: Its derivatives can be explored for use in agricultural applications, particularly as pesticides or herbicides.

As scientists continue to explore the vast landscape of urea derivatives, 1-carbamoyl-3-[2-(4-methoxyphenyl)ethyl]urea serves as a reminder of the compound's versatility and the exciting discoveries that await. With its unique structural features and significant potential, this compound is poised to contribute to advancements in multiple scientific arenas.

Synonyms
1-(p-Methoxyphenethyl)biuret
BIURET, 1-(p-METHOXYPHENETHYL)-
BRN 2745536
6774-20-5
DTXSID70218019
DTXCID40140510