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Carbaryl

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Identification
Molecular formula
C12H11ClNO2
CAS number
63-25-2
IUPAC name
2-(dimethylamino)ethyl N-(2-chloro-6-methyl-phenyl)carbamate
State
State

At room temperature, Carbaryl is typically found as a solid.

Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
221.68g/mol
Molar mass
201.6580g/mol
Density
1.1140g/cm3
Appearence

Carbaryl is a white crystalline solid. It can appear as a colorless solid when pure.

Comment on solubility

Solubility of 2-(dimethylamino)ethyl N-(2-chloro-6-methyl-phenyl)carbamate

The compound 2-(dimethylamino)ethyl N-(2-chloro-6-methyl-phenyl)carbamate, with its complex structure, exhibits intriguing solubility characteristics. Solubility is a vital aspect in understanding how a chemical behaves in various environments, and this compound is no exception.

Key Solubility Insights

  • Polar Features: The presence of a dimethylamino group contributes to the polar nature of the compound, suggesting potential solubility in polar solvents such as water and alcohols.
  • Non-Polar Characteristics: The aromatic 2-chloro-6-methyl-phenyl moiety introduces some hydrophobicity, which may limit its solubility in strongly polar solvents.
  • Overall Solubility: While the compound is likely to have moderate solubility in water, it could show enhanced solubility in organic solvents like acetone or ethanol due to the combined effects of oil and water interactions.

Overall, one can hypothesize that the solubility of this compound is influenced by its structural components, resulting in a balance between its polar and non-polar characteristics. As with many organic compounds, it’s always recommended to conduct empirical tests to determine the actual solubility in various solvents under specific conditions.

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethyl N-(2-chloro-6-methyl-phenyl)carbamate

This compound, known as a carbamate derivative, has garnered attention in both industrial and pharmaceutical settings due to its diverse applications and intriguing chemical structure. Here are some interesting facts:

  • Mechanism of Action: The carbamate moiety plays a crucial role in inhibiting enzymes like acetylcholinesterase, which is vital for nerve function. This makes compounds like this one valuable in the development of certain medications.
  • Pesticide Potential: With its ability to inhibit key biological pathways, this compound is explored for its potential use in agriculture as an effective pesticide, ensuring better crop protection.
  • Structural Diversity: The presence of both a dimethylamino group and a chloro-substituted aromatic ring allows for the fine-tuning of the compound's properties, making it a subject of interest in medicinal chemistry.
  • Research Applications: Due to its unique structure, it has been studied in various research initiatives focused on neurological disorders and the development of neuroprotective agents.
  • Environmental Impact: As with many carbamates, understanding its degradation products and toxicity is important in assessing its long-term environmental impact, contributing to discussions on sustainable chemical practices.

To quote a notable chemist, “The intricacies of carbamate chemistry open doors to innovations in both our understanding of nature and the development of new technologies.” This encapsulates the potential implications of compounds like 2-(dimethylamino)ethyl N-(2-chloro-6-methyl-phenyl)carbamate in shaping future chemical research.

In summary, the compound’s multifaceted properties and applications signal its importance in the realms of both chemistry and biology, making it a fascinating subject for study and exploration in ongoing research.

Synonyms
AKOS024335519
2-(dimethylamino)ethyl 2-chloro-6-methylphenylcarbamate