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Diethylcarbamazine (DEC)

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Identification
Molecular formula
C10H21ClN2O2S
CAS number
90-89-1
IUPAC name
diethyl-[2-[(5-methoxy-1,3-benzoxazol-2-yl)sulfanyl]ethyl]ammonium;chloride
State
State

At room temperature, diethylcarbamazine chloride typically exists in a solid state, appearing as a white crystalline powder.

Melting point (Celsius)
138.50
Melting point (Kelvin)
411.65
Boiling point (Celsius)
153.00
Boiling point (Kelvin)
426.15
General information
Molecular weight
235.76g/mol
Molar mass
235.7640g/mol
Density
1.1683g/cm3
Appearence

This compound typically appears as a white or off-white crystalline powder. It is odourless to slight characteristic smell.

Comment on solubility

Solubility of Diethyl-[2-[(5-methoxy-1,3-benzoxazol-2-yl)sulfanyl]ethyl]ammonium;chloride

The solubility of diethyl-[2-[(5-methoxy-1,3-benzoxazol-2-yl)sulfanyl]ethyl]ammonium;chloride is a topic of interest, given its unique structure and functional groups. This compound, as a quaternary ammonium salt, typically exhibits solubility characteristics governed by several factors:

  • Polar Nature: The presence of the ammonium group contributes significantly to the polarity of the molecule, enhancing its solubility in polar solvents, particularly water.
  • Chloride Ion Influence: The chloride ion, being a small and highly soluble anion, aids in the dissolution process, promoting a favorable interaction with the solvent.
  • Hydrophilic Aromatic Ring: The methoxy functional group located on the benzoxazole moiety can also engage in hydrogen bonding, further increasing solubility in polar media.

In general, it is likely that diethyl-[2-[(5-methoxy-1,3-benzoxazol-2-yl)sulfanyl]ethyl]ammonium;chloride is:

  • Highly soluble in water, attributed to its ionic nature and polar functional groups.
  • Less soluble in nonpolar solvents, due to insufficient interactions with such environments.

In summary, the solubility of this compound can be considered favorable for applications in aqueous contexts, making it a potential candidate for use in various chemical and biological systems. Remember, the specific solubility can vary based on external conditions such as temperature and pH levels, which can be crucial for practical applications.

Interesting facts

Interesting Facts about Diethyl-[2-[(5-methoxy-1,3-benzoxazol-2-yl)sulfanyl]ethyl]ammonium Chloride

Diethyl-[2-[(5-methoxy-1,3-benzoxazol-2-yl)sulfanyl]ethyl]ammonium chloride is a compound of significant interest due to its unique structure and potential applications. Here are some fascinating insights:

  • Medicinal Chemistry: This compound has shown promise in the field of medicinal chemistry, especially in the development of pharmaceuticals targeting specific biological pathways.
  • Biological Activity: The presence of the benzoxazole moiety is particularly noteworthy as benzoxazoles are known for their diverse biological activities, including antimicrobial, anti-inflammatory, and anticancer properties.
  • Ion Exchange Properties: As a quarternary ammonium salt, it exhibits unique ion exchange properties, which can be valuable in various applications including water treatment and separation techniques.
  • Research Applications: This compound may serve as a valuable tool in chemical biology. Its sulfanyl group enhances its reactivity, making it suitable for probing and modifying biomolecules.
  • Synthesis Challenges: The synthesis of this compound can be complex, often requiring careful selection of reagents and conditions to ensure the formation of the desired product without side reactions.

In summary, diethyl-[2-[(5-methoxy-1,3-benzoxazol-2-yl)sulfanyl]ethyl]ammonium chloride represents a fascinating intersection of organic synthesis and biological research, highlighting the potential for innovative applications in chemistry and medicine. As researchers continue to explore its properties and functions, this compound may play a transformative role in various fields.

Synonyms
2-((2-(Diethylamino)ethyl)thio)-5-methoxybenzoxazole hydrochloride
14627-03-3
BENZOXAZOLE, 2-((2-(DIETHYLAMINO)ETHYL)THIO)-5-METHOXY-, MONOHYDROCHLORIDE