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Carbofuran

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Identification
Molecular formula
C12H15Cl2NO2
CAS number
1563-66-2
IUPAC name
2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate
State
State
Carbofuran appears as a solid at room temperature. It is generally stable under normal conditions and does not sublimate or disintegrate easily, maintaining its structural integrity in typical storage or usage environments.
Melting point (Celsius)
152.00
Melting point (Kelvin)
425.15
Boiling point (Celsius)
373.40
Boiling point (Kelvin)
646.55
General information
Molecular weight
221.11g/mol
Molar mass
221.1110g/mol
Density
1.2130g/cm3
Appearence

Carbofuran is typically a white crystalline solid. It is notable for its distinct powdery texture that is characteristic of many carbamate insecticides. Often used in agricultural settings, it is commonly available in a finely-ground form, allowing for easy mixing with other substances or formulations.

Comment on solubility

Solubility of 2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate

The solubility of 2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate is an intriguing aspect of this compound, given its chemical structure. Its solubility can be impacted by several factors:

  • Polarity: The presence of both hydrophilic (diethylamino group) and hydrophobic (3,5-dichlorophenyl group) features in its structure leads to varied solubility behavior.
  • Solvent Interactions: This compound is typically more soluble in organic solvents due to its non-polar characteristics, while its solubility in water is often limited.
  • pH Dependence: Changes in pH can alter the ionization state of the amino group, potentially increasing its water solubility in more basic conditions.

As with many similar compounds, “the solubility phenomenon is vastly influenced by molecular interactions and the surrounding environment.” Therefore, understanding the conditions under which this compound dissolves is essential for applications in various fields, such as pharmaceuticals and agrochemicals.

In summary, while 2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate displays limited water solubility, its behavior in organic solvents reveals greater potential, making it a compound of interest in chemical formulations.

Interesting facts

Interesting Facts about 2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate

2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate, commonly known as a potent inhibitor, is a compound that reveals fascinating insights into chemical functionality and applications in various fields.

Key Features

  • Biological Activity: This compound exhibits significant biological activity, making it valuable in pharmaceutical research. Its mechanism often involves interactions with neurotransmitter systems, influencing a variety of biological responses.
  • Pest Control: Due to its carbamate structure, it can function as an insecticide, illustrating its applicability in agriculture. Carbamates are known for their effectiveness against a wide range of pests.
  • Synthetic Pathways: The synthesis of this compound involves multi-step organic reactions which could include nucleophilic substitutions and coupling reactions, making it a prime candidate for educational purposes in organic chemistry courses.
  • Structure-Activity Relationship (SAR): The modification of the diethylamino and dichlorophenyl portions can lead to variations in biological activity, shedding light on the importance of SAR in drug design.

Anecdotal Insights

As a chemistry student, exploring compounds like this can ignite a passion for research. Consider this interesting quote from a seasoned chemist: "Understanding the intricacies of molecular interactions opens doors to innovation." This highlights why studying such compounds is not merely academic but can lead to real-world solutions.

Ultimately, 2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate embodies the intersection of chemistry, biology, and practical applications, encouraging future scientists to unlock the potential hidden within its structure.

Synonyms
NSC379373
NSC-379373