Skip to main content

Carbaryl

ADVERTISEMENT
Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(1-methyl-2-nitro-propyl) N-phenylcarbamate
State
State
Carbaryl is typically a solid at room temperature, existing as colorless crystals which may be slightly colored if impurities are present.
Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2200g/mol
Density
1.2300g/cm3
Appearence
Carbaryl primarily appears as a colorless crystalline solid. When pure, it is white in color and may sometimes appear as a solid that is slightly colored.
Comment on solubility

Solubility of (1-methyl-2-nitro-propyl) N-phenylcarbamate

The solubility of (1-methyl-2-nitro-propyl) N-phenylcarbamate can be influenced by several factors, including its molecular structure and the nature of the solvent. Here are some key points to consider:

  • Polarity: This compound contains polar functional groups such as the nitro group and the carbamate linkage, which may enhance its solubility in polar solvents.
  • Hydrogen Bonding: The presence of hydrogen bond donors and acceptors in the carbamate structure can facilitate solubility in protic solvents, such as water.
  • Hydrophobic Interactions: The 1-methyl-2-nitro-propyl moiety introduces hydrophobic characteristics, which might limit solubility in highly polar solvents.
  • Temperature Dependence: Solubility is often temperature-dependent; thus, increasing temperature can enhance the solubility of this compound in suitable solvents.

In summary, while (1-methyl-2-nitro-propyl) N-phenylcarbamate may exhibit some degree of solubility in polar solvents due to its functional groups, its overall solubility is a balance between its hydrophilic and hydrophobic parts. The application of this compound will therefore be contingent on the choice of solvent and environmental conditions.

Interesting facts

Interesting Facts about (1-methyl-2-nitro-propyl) N-phenylcarbamate

(1-methyl-2-nitro-propyl) N-phenylcarbamate is a fascinating compound that showcases the intricate interplay between organic chemistry and applications in various fields. Here are some intriguing aspects of this compound:

  • Structural Complexity: This compound features a unique combination of a nitro group and a carbamate moiety, which gives it distinctive chemical properties. The presence of the nitro group introduces potential for reactivity through electrophilic substitution reactions.
  • Pesticide Potential: Compounds like (1-methyl-2-nitro-propyl) N-phenylcarbamate may play roles in agrochemistry, particularly in the development of pesticides. The carbamate functional group is known for its insecticidal properties, affecting the nervous system of insects.
  • Medicinal Chemistry: The study of carbamate derivatives is significant in medicinal chemistry as many exhibit pharmacological activities. Research into derivatives of this compound may yield useful insights into potential therapeutic applications.
  • Synthesis Strategies: The synthesis of this compound can demonstrate various organic reactions, such as nucleophilic substitutions and esterifications, making it a valuable example in educational settings.
  • Environmental Considerations: Like many chemical compounds, understanding the environmental impact of (1-methyl-2-nitro-propyl) N-phenylcarbamate is critical. Research into its degradation and toxicity is important for assessing its risk in ecological systems.

In conclusion, (1-methyl-2-nitro-propyl) N-phenylcarbamate represents a niche within organic chemistry that interlinks structural versatility with practical applications in agriculture and pharmaceuticals. Its complex nature invites a deeper investigation into its properties and potential uses.

Synonyms
6526-61-0
BRN 2735916
2-Nitroisobutyl-N-phenylcarbamate
CARBAMIC ACID, PHENYL-, (1-METHYL-2-NITROPROPYL) ESTER
DTXSID40983863
3-Nitrobutan-2-yl hydrogen phenylcarbonimidate