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Carbaryl

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

At room temperature, Carbaryl is typically found in a solid state.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
201.67g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a white crystalline solid. It may present in powder form and is usually odorless. Over time and under certain conditions, its color can turn to a yellowish tint due to exposure or impurities.

Comment on solubility

Solubility of (1-methylpyrrolidin-2-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate

The solubility of (1-methylpyrrolidin-2-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate in various solvents is a topic of interest due to its implications in pharmaceutical applications and chemical behavior. Understanding its solubility can help in optimizing formulations and reactions.

Factors Influencing Solubility

Several factors play a critical role in determining the solubility of this compound:

  • Polarity: As a carbamate, the presence of polar functional groups can enhance solubility in polar solvents, such as water or alcohol.
  • Temperature: Generally, an increase in temperature can lead to increased solubility for many organic compounds. However, this can vary based on the specific interactions present.
  • pH: The acidity or basicity of the solvent can also impact the ionization state of the compound, thereby influencing its solubility.
  • Solvent Structure: The molecular structure of the solvent can interact differently with the compound, affecting solubility outcomes.

Predicted Solubility

While specific solubility data may be limited, it can be suggested that:

  • The compound might be more soluble in organic solvents such as ethanol or acetone due to the hydrophobic carbon chain.
  • In water, solubility may be low but could be enhanced through modifications or in the presence of co-solvents.

In conclusion, the solubility of (1-methylpyrrolidin-2-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate is influenced by its chemical structure and the nature of the solvent. Understanding these factors is crucial for effectively utilizing this compound in various applications.

Interesting facts

Interesting Facts about (1-methylpyrrolidin-2-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate

(1-methylpyrrolidin-2-yl)methyl N-(2-chloro-6-methyl-phenyl)carbamate is an intriguing chemical compound with various applications in the field of medicinal chemistry. Here are some notable points:

  • Mechanism of Action: This compound operates primarily as a carbamate, which means it can inhibit certain enzymes, thereby modulating biological pathways. Its structure indicates potential activity in the central nervous system.
  • Synthetic Pathways: The synthesis of this compound often involves the use of pyrrolidin-2-yl and chloro-substituted aryl structures, showcasing the versatility of organic synthesis techniques such as nucleophilic substitutions and coupling reactions.
  • Potential Applications: Due to its unique structure, this compound may be explored for its therapeutic effects in treating neurological disorders, pain relief, or as an insecticide in agricultural practices.
  • Environmental Considerations: As with many chemicals featuring a chlorinated moiety, researchers are keen to assess the environmental impact and degradation pathways of this compound in nature.
  • Research Interest: The combination of the pyrrolidine ring with a chloro-substituted aromatic side chain has attracted research for its potential to yield new pharmaceuticals, particularly in drug discovery programs targeting specific receptors.

As we continue to explore this compound, it paves the way for potential advancements in various fields, causing scientists to ask the question: what new therapeutic possibilities could stem from understanding and manipulating its properties?

Synonyms
2-Chloro-6-methylcarbanilic acid (1-methyl-2-pyrrolidinyl)methyl ester
17829-06-0
BRN 1482005
CARBANILIC ACID, 2-CHLORO-6-METHYL-, (1-METHYL-2-PYRROLIDINYL)METHYL ESTER
DTXSID60939064
(1-Methylpyrrolidin-2-yl)methyl hydrogen (2-chloro-6-methylphenyl)carbonimidate