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Dyclonine

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Identification
Molecular formula
C18H27Cl2NO2
CAS number
586-60-7
IUPAC name
2-(diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate
State
State

At room temperature, Dyclonine is in a solid state, typically utilized in lozenge or solution forms for medical applications to deliver its numbing effects efficiently.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.00
Boiling point (Celsius)
426.60
Boiling point (Kelvin)
699.80
General information
Molecular weight
328.22g/mol
Molar mass
328.2170g/mol
Density
1.3110g/cm3
Appearence

Dyclonine generally appears as a white, crystalline powder. It has no distinct odor, making it suitable for pharmaceutical formulations. Its crystalline nature indicates that it is a solid at room temperature.

Comment on solubility

Solubility of 2-(diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate

The solubility of 2-(diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate, a carbamate compound, exhibits interesting characteristics due to its specific molecular structure. Understanding its solubility behavior is crucial in various applications including pharmaceuticals, agrochemicals, and chemical synthesis. Here are some key points to consider:

  • Polar vs. Non-Polar: This compound possesses both polar and non-polar characteristics because of the diethylamino group and the dichlorophenyl ring. This dual nature often leads to moderate solubility in polar solvents like water, as well as non-polar solvents such as organic hydrocarbons.
  • Temperature Dependence: Its solubility is likely to be temperature-dependent, with increased temperatures generally enhancing solubility in both types of solvents.
  • pH Influence: The pH of the solvent can significantly affect solubility as well, especially since it has basic amine groups that might become protonated in acidic environments, enhancing solubility in aqueous solutions.
  • Intermolecular Interactions: The ability to form hydrogen bonds with water molecules can increase solubility in polar solvents, while the steric hindrance of the diethylamino group may create limitations in forming such bonds.

Overall, the solubility of 2-(diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate combines various factors, making it a fascinating compound for detailed study. As Jacques E. D. Salm once noted, "The behavior of compounds in solution is a mirror reflecting their intrinsic nature." Exploring the solubility of such compounds provides profound insights into their potential applications.

Interesting facts

Interesting Facts about 2-(Diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate

2-(Diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate is a remarkable compound that has attracted attention in various fields, particularly in pharmacology and agricultural chemistry. Here are some intriguing aspects to consider:

  • Functional Group Diversity: This compound features a carbamate functional group, which is known for its role in numerous biological and chemical processes. Carbamates can serve both as pesticides and pharmaceutical agents.
  • Synthetic Versatility: The structure of 2-(diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate allows for a variety of synthetic strategies for its formation. The presence of diethylamino and dichlorophenyl groups enhances the compound's reactivity and potential for modification, making it a valuable intermediate in chemical synthesis.
  • Biological Activity: Compounds of this nature often exhibit significant biological activities. The presence of the dichlorophenyl group can enhance toxicity and efficacy against certain pests or pathogens, which is particularly useful in developing agrochemicals.
  • Potential in Drug Development: Given the properties of carbamates and their interactions with biological systems, there is ongoing research into the use of similar compounds in drug development. The unique structure could lead to innovative therapeutic agents with specific target profiles.
  • Environmental Considerations: As with many chemical compounds used in agriculture, understanding the environmental impact of 2-(diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate is crucial. Studies into its degradation and metabolism are essential for assessing its safety and sustainability.
  • Quote on Chemical Innovation: "Every chemical compound has a story, and their interactions with life are chapters waiting to be explored." This sentiment emphasizes the dynamic nature of research surrounding compounds like this one.

In summary, 2-(diethylamino)ethyl N-(2,6-dichlorophenyl)carbamate exemplifies the intricate interplay of chemistry and biology. Its diverse functional groups and potential applications make it a compound worth studying, whether you are a student, researcher, or industry professional.

Synonyms
NSC379381
AKOS024336653
NSC-379381
2-(diethylamino)ethyl 2,6-dichlorophenylcarbamate