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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[3-(but-2-enoylamino)phenyl] N-methylcarbamate
State
State
At room temperature, carbaryl is typically found in a solid state. It has limited solubility in water, which affects its handling and application as an insecticide. It is more soluble in organic solvents.
Melting point (Celsius)
142.30
Melting point (Kelvin)
415.45
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence
Carbaryl is a crystalline solid that is generally white or colorless. It is often found in powder or granular form when used as an insecticide. In commercial preparations, it may appear off-white due to impurities commonly associated with industrial production processes.
Comment on solubility

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

The solubility of [3-(but-2-enoylamino)phenyl] N-methylcarbamate can be influenced by several factors, making it a compound of interest in both scientific research and practical applications.

Key Factors Affecting Solubility:

  • Polarity: The presence of functional groups such as the carbamate moiety may contribute to polarity, affecting its interaction with solvents.
  • Temperature: Increased temperatures often enhance solubility for many compounds; thus, experimenting at different temperatures can provide insights.
  • pH Levels: The solubility can be altered by pH, especially due to the amine functionality which can undergo protonation in acidic conditions.
  • Solvent Choice: Nonpolar versus polar solvents can dramatically alter solubility outcomes. For instance, polar solvents like water or alcohols may dissolve the compound more readily than nonpolar hydrocarbons.

Understanding the solubility of [3-(but-2-enoylamino)phenyl] N-methylcarbamate can lead to improved formulation techniques and applications in various fields, such as pharmaceuticals and agrochemicals. As a takeaway, it is crucial to consider the aforementioned factors in order to determine the optimal conditions for solubility.

Interesting facts

Interesting Facts about [3-(but-2-enoylamino)phenyl] N-methylcarbamate

[3-(but-2-enoylamino)phenyl] N-methylcarbamate is a fascinating compound that belongs to the class of carbamates, which are widely recognized for their diverse biological activities. Here are some intriguing facts about this compound:

  • Biological Relevance: This compound may serve as an important building block in medicinal chemistry, particularly in the development of pharmaceuticals that target specific biological pathways.
  • Structural Versatility: The presence of the but-2-enoylamino group introduces interesting reactivity opportunities, allowing it to participate in various chemical reactions, including polymerization and conjugation reactions.
  • Enzyme Interaction: Carbamates are known for their ability to interact with various enzymes, including acetylcholinesterase, which plays a crucial role in neurotransmission. Studying this compound might provide insights into its potential inhibitory effects.
  • Synthetic Pathways: The synthesis of [3-(but-2-enoylamino)phenyl] N-methylcarbamate showcases an elegant intersection of organic synthesis techniques, highlighting the creativity and innovation required in modern chemistry.
  • Potential Applications: Researchers are exploring its potential use in agricultural chemistry as a pesticide or herbicide due to the inherent activity of carbamates in these applications.

As a compound that bridges various fields of chemistry, [3-(but-2-enoylamino)phenyl] N-methylcarbamate exemplifies the complexity and richness of chemical science. Its study can open pathways to new discoveries in drug design, agricultural solutions, and fundamental chemistry.