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Clocortolone Pivalate

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Identification
Molecular formula
C10H14ClNO2
CAS number
115-32-2
IUPAC name
2-(diethylamino)ethyl N-(4-chlorophenyl)carbamate
State
State

At room temperature, it is generally a solid compound.

Melting point (Celsius)
48.00
Melting point (Kelvin)
321.15
Boiling point (Celsius)
373.00
Boiling point (Kelvin)
646.15
General information
Molecular weight
225.68g/mol
Molar mass
225.7000g/mol
Density
1.1152g/cm3
Appearence

This compound typically appears as a colorless to pale yellow crystalline solid. It may sometimes be found as a powder depending on its formulation and processing.

Comment on solubility

Solubility of 2-(diethylamino)ethyl N-(4-chlorophenyl)carbamate

The solubility of 2-(diethylamino)ethyl N-(4-chlorophenyl)carbamate can be understood through various influencing factors:

  • Polarity: This compound exhibits a degree of polarity due to the presence of the diethylamino group, which can enhance solubility in polar solvents.
  • Functional Groups: The -N-(4-chlorophenyl) moiety can interact with solvents through hydrogen bonding and dipole-dipole interactions, potentially increasing its solubility in suitable environments.
  • Solvent Compatibility: It may be more soluble in organic solvents, especially those with polar characteristics, such as methanol or ethanol, while demonstrating lesser solubility in non-polar solvents such as hexane.

Overall, while the compound shows useful features that can facilitate solubility, definitive solubility will depend on precise conditions including temperature and the specific nature of the solvent.

As a closing remark, understanding the solubility of chemical compounds like this one is crucial in fields such as pharmaceuticals and agricultural chemistry, where solubility can impact bioavailability and efficacy.

Interesting facts

Interesting Facts about 2-(Diethylamino)ethyl N-(4-chlorophenyl)carbamate

2-(Diethylamino)ethyl N-(4-chlorophenyl)carbamate is a fascinating compound that plays a significant role in chemistry and pharmacology. Here are some intriguing aspects of this compound:

  • Class of Compounds: This compound belongs to the class of carbamates, which are widely studied for their biological activities and potential therapeutic applications.
  • Applications: It is primarily explored for its use as a pesticide and also in the development of pharmaceuticals, showcasing its versatility in both agricultural and medical fields.
  • Mechanism of Action: Carbamates generally act as acetylcholinesterase inhibitors, which means they can interfere with the breakdown of the neurotransmitter acetylcholine. This can lead to prolonged nerve signal transmission.
  • Structure-Activity Relationship: The presence of the diethylamino group significantly contributes to its potency and selectivity, making it an interesting subject for synthetic chemists aiming to develop new derivatives with enhanced activity.
  • Historical Context: Carbamates have been a topic of research since the introduction of pesticides in agriculture, leading to a rich history of study and evolution in chemical synthesis.
  • Safety and Environmental Impact: The use of carbamates must be carefully managed due to their potential environmental effects and toxicity to non-target organisms, prompting ongoing research in safer alternatives.

The exploration of 2-(diethylamino)ethyl N-(4-chlorophenyl)carbamate not only enriches our understanding of chemical interactions but also opens doors to innovative applications in different fields. As emphasized in scientific discussions, the balance between efficacy and safety remains paramount in the continued use of compounds like this one.

Synonyms
2-(diethylamino)ethyl N-(4-chlorophenyl)carbamate
107410-36-6
667-440-9
RefChem:460581
NSC202642
AKOS024335465
NSC-202642