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Carbaryl

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Identification
Molecular formula
C12H11ClNO2
CAS number
63-25-2
IUPAC name
(2-chloro-3,5-dimethyl-phenyl) N-methylcarbamate
State
State

Carbaryl is a solid at room temperature.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
182.00
Boiling point (Kelvin)
455.15
General information
Molecular weight
201.66g/mol
Molar mass
201.6600g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a white crystalline solid.

Comment on solubility

Solubility of (2-chloro-3,5-dimethyl-phenyl) N-methylcarbamate

The solubility of (2-chloro-3,5-dimethyl-phenyl) N-methylcarbamate can be influenced by various factors, including its chemical structure and environmental conditions. This compound typically demonstrates:

  • Polar Characteristics: The presence of the N-methylcarbamate functional group often leads to increased interactions with polar solvents, highlighting its potential solubility in water.
  • Hydrophobic Interactions: The chlorinated aromatic ring in its structure may introduce hydrophobic properties, which could decrease solubility in less polar solvents.
  • Temperature Effects: As with many organic compounds, solubility can vary with temperature; it is essential to consider the solubility dynamics across different temperatures.

In general, it is crucial to evaluate solubility through empirical data as it varies widely among different solvents and concentrations. Testing solubility in multiple solvents allows for a comprehensive understanding of (2-chloro-3,5-dimethyl-phenyl) N-methylcarbamate's behavior in various applications. Ultimately, understanding solubility is indispensable for predicting compound interactions and reactivity in chemical processes.

Interesting facts

Exploring (2-chloro-3,5-dimethyl-phenyl) N-methylcarbamate

(2-chloro-3,5-dimethyl-phenyl) N-methylcarbamate, commonly referred to as a member of the carbamate class, holds intriguing properties and applications. This compound is particularly notable due to its structural features which contribute to its multifaceted roles in various fields.

Key Characteristics

  • Insecticidal Properties: This compound is often utilized in agriculture as an insecticide. Its ability to inhibit certain biochemical pathways in pests makes it an essential tool for pest management.
  • Structural Versatility: The incorporation of the chloro and methyl groups allows for a diverse range of reactivity. Aromatic compounds like this one often exhibit stability while also providing sites for further chemical modification.
  • Environmental Considerations: As with many agrochemicals, its environmental impact is a topic of ongoing research. Understanding its degradation pathways and potential accumulation in ecosystems is critical.

Chemical Reactions

This compound engages in various chemical reactions, including:

  1. Nucleophilic Substitution: The chloro group allows for nucleophilic attacks, facilitating the synthesis of more complex molecules.
  2. Hydrolysis: Under certain conditions, the carbamate group can undergo hydrolysis, leading to the formation of corresponding acids and alcohols.

Research and Applications

Recent studies have highlighted the potential of (2-chloro-3,5-dimethyl-phenyl) N-methylcarbamate in:

  • Crop Protection: Enhancing crop yields by controlling pest populations in an eco-friendly manner.
  • Medicinal Chemistry: Investigating its analogs and derivatives for potential therapeutic applications.

As scientists continue to unravel the complexities surrounding this compound, it serves as a reminder of the critical balance between agricultural advancement and environmental stewardship. Understanding the behavior and impacts of such compounds is essential for sustainable practices in chemistry and agriculture alike.

Synonyms
Upjohn 12927
2425-08-3
BRN 2973021
Methylcarbamic acid 2-chloro-3,5-xylyl ester
CARBAMIC ACID, METHYL-, 2-CHLORO-3,5-XYLYL ESTER
DTXSID90178944
DTXCID50101435
(2-Chloro-3,5-dimethylphenyl)n-methylcarbamate