Skip to main content

Diallylchoroacetamide monohydrochloride

ADVERTISEMENT
Identification
Molecular formula
C12H17NCl2O
CAS number
145783-14-8
IUPAC name
diallyl-[2-(3-chloroanilino)-2-oxo-ethyl]ammonium;chloride
State
State

At room temperature, the compound remains in a solid state, owing to its crystalline structure.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
306.25g/mol
Molar mass
306.2500g/mol
Density
1.1560g/cm3
Appearence

This compound appears as a white crystalline powder, exhibiting typical characteristics of chlorinated ammonium compounds.

Comment on solubility

Solubility of Diallyl-[2-(3-chloroanilino)-2-oxo-ethyl]ammonium Chloride

Diallyl-[2-(3-chloroanilino)-2-oxo-ethyl]ammonium chloride is an interesting compound when it comes to solubility. Here are some key points to consider:

  • Polar Nature: Given its ammonium component, this compound exhibits a significant polar character. This often enhances its solubility in polar solvents.
  • Chloride Ion Influence: The presence of chloride ions can increase the solubility of the compound in water, as these ions readily dissociate and help to stabilize interactions with water molecules.
  • Organic Solvents: The diallyl group, being non-polar to some extent, may limit solubility in purely polar solvents, making it more soluble in a mixture of solvents or in organic solvents like ethanol or methanol.

In general, one can anticipate that diallyl-[2-(3-chloroanilino)-2-oxo-ethyl]ammonium chloride is soluble in polar solvents but may show variable solubility in organic solvents. This dual character makes it a fascinating subject for further studies on solubility dynamics.

Interesting facts

Interesting Facts about Diallyl-[2-(3-chloroanilino)-2-oxo-ethyl]ammonium Chloride

Diallyl-[2-(3-chloroanilino)-2-oxo-ethyl]ammonium chloride, often abbreviated as DAC, is a fascinating compound that has caught the attention of scientists for several reasons. This compound blends an organic functional group with a quaternary ammonium structure, making it a unique subject for study in both organic and medicinal chemistry.

Key Characteristics:

  • Versatile Applications: DAC is known for its use in various fields including pharmaceuticals, where it helps in drug formulation and delivery due to its solubility and reactivity.
  • Antimicrobial Properties: The chlorinated aniline portion of the compound contributes to its potential antimicrobial activity, which is valuable in developing new antibacterial agents.
  • Polymerization Potential: Its diallyl group serves as a precursor for polymer formation, enabling the synthesis of new materials with desired properties.

Scientists are particularly interested in the compound's structure because it demonstrates how varied substituents can influence biological activity; as one researcher noted, "The incorporation of halogens can significantly enhance the interaction with biological targets." This indicates that subtle changes at the molecular level can lead to profound effects on activity and utility.

Research Implications:

As ongoing research delves deeper into this compound, chemists are keen to uncover its mechanisms of action and potential therapeutic applications. The synthesis methods and reactivity patterns of DAC offer rich ground for innovation and discovery in the realms of drug design and materials science.

In conclusion, Diallyl-[2-(3-chloroanilino)-2-oxo-ethyl]ammonium chloride is more than just a simple compound—it represents a crossroads of organic chemistry, material science, and medicinal applications, underscoring the intricate beauty and complexity of chemical research.

Synonyms
3'-Chloro-2-diallylaminoacetanilide hydrochloride
ACETANILIDE, 3'-CHLORO-2-(DIALLYLAMINO)-, MONOHYDROCHLORIDE
21340-42-1
RefChem:315776