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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[2-hydroxy-3-(2-methoxyphenoxy)propyl] N-aminocarbamate
State
State

At room temperature, Carbaryl exists as a crystalline solid.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
201.22g/mol
Molar mass
201.2200g/mol
Density
1.2300g/cm3
Appearence

Carbaryl typically appears as a white crystalline solid.

Comment on solubility

Solubility of [2-hydroxy-3-(2-methoxyphenoxy)propyl] N-aminocarbamate

The solubility of [2-hydroxy-3-(2-methoxyphenoxy)propyl] N-aminocarbamate can be influenced by several factors, making it an interesting compound to investigate. Here are some key points regarding its solubility:

  • Polarity: The presence of functional groups, such as the hydroxyl group and the methoxyphenyl moiety, suggests that the compound could have moderate polarity. As a result, it may exhibit reasonable solubility in polar solvents such as water and alcohols.
  • Hydrogen Bonding: The ability to form hydrogen bonds due to the hydroxyl group can enhance solubility in water. Compounds that can engage in hydrogen bonding are often more soluble in polar solvents.
  • Solvent Interaction: Solubility may vary significantly depending on the nature of the solvent used. For example, solvents like ethanol or methanol may solubilize this compound better than non-polar solvents.
  • Temperature Influence: Temperature can play a crucial role in solubility; increasing the temperature may enhance solubility for many compounds, including [2-hydroxy-3-(2-methoxyphenoxy)propyl] N-aminocarbamate.

In summary, while specific quantitative solubility data may be necessary for practical applications, the characteristics of this compound suggest a potential for reasonable solubility in suitable polar solvents. Understanding its solubility behavior is crucial for predicting its performance in different chemical environments.

Interesting facts

About [2-hydroxy-3-(2-methoxyphenoxy)propyl] N-aminocarbamate

[2-hydroxy-3-(2-methoxyphenoxy)propyl] N-aminocarbamate is an intriguing compound that possesses a variety of interesting features, primarily due to its unique structural composition. Here are some highlights:

  • Amidic Functionality: The presence of the N-aminocarbamate group offers potential for interesting properties, such as bioactivity and application in medicinal chemistry. These compounds often exhibit herbicidal or insecticidal properties, which makes them valuable in agriculture.
  • Potential Applications: With its specific functional groups, this compound can be useful in the synthesis of more complex molecules, which could be relevant in drug design. Researchers are continuously exploring its potential applications in various fields including pharmaceuticals and agrochemicals.
  • Synthetic Versatility: The structure allows for modifications at different sites, which can lead to an array of derivatives. This versatility can be leveraged to tailor the properties of the compound for specific needs or desired functionalities.
  • Biochemical Interaction: The hydroxy and methoxy groups may influence the compound’s solubility and its interaction with biological targets, crucial for pharmacological studies.
  • Research Interest: Studies on similar compounds have highlighted their roles in cellular signaling processes, making them fascinating subjects for scientists in the fields of biochemistry and molecular biology.

Conclusion

In summary, [2-hydroxy-3-(2-methoxyphenoxy)propyl] N-aminocarbamate stands as a compound of considerable interest due to its potential applications and biochemical significance. As researchers delve deeper into its properties, we may uncover new insights that could lead to valuable innovations in science and technology.

Synonyms
3-(o-Methoxyphenoxy)-2-hydroxypropyl aminocarbamate
16929-74-1
BRN 2538813
1,2-Propanediol, 3-(o-methoxyphenoxy)-, carbazate
CARBAZIC ACID, 2-HYDROXY-3-(o-METHOXYPHENOXY)PROPYL ESTER
DTXSID10937616
2-Hydroxy-3-(2-methoxyphenoxy)propyl hydrogen carbonohydrazonate