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Etamicastat

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Identification
Molecular formula
C13H21ClN2O
CAS number
117527-57-2
IUPAC name
(2-anilino-2-oxo-ethyl)-diethyl-ammonium;chloride
State
State

At room temperature, etamicastat is in a solid state.

Melting point (Celsius)
172.00
Melting point (Kelvin)
445.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
308.83g/mol
Molar mass
308.8290g/mol
Density
1.0700g/cm3
Appearence

Etamicastat appears as a white crystalline solid. It is typically supplied in solid form and is known for its stability when stored under recommended conditions.

Comment on solubility

Solubility Overview

The compound known as (2-anilino-2-oxo-ethyl)-diethyl-ammonium;chloride exhibits specific properties within various solvents.


Key Features of Solubility:

  • Water Solubility: This compound is expected to be soluble in water due to the presence of the ammonium chloride component, which typically enhances solubility.
  • Polar Solvents: Solubility may be favorable in polar solvents, making solvents such as methanol and ethanol suitable options for dissolving this compound.
  • Non-polar Solvents: Its solubility in non-polar solvents is likely to be minimal, as the presence of ionic and polar features typically limits compatibility with such environments.

According to standard solubility principles, the phrase "like dissolves like" is particularly relevant here; hence, this compound may show better solubility in media that share similar chemical characteristics to its structure. Overall, the behavior of (2-anilino-2-oxo-ethyl)-diethyl-ammonium;chloride in various solvents reflects its complex interactions attributable to its ionic and molecular characteristics.

Interesting facts

Interesting Facts About (2-anilino-2-oxo-ethyl)-diethyl-ammonium;chloride

(2-anilino-2-oxo-ethyl)-diethyl-ammonium;chloride, often referred to simply as a quaternary ammonium salt, is a fascinating compound with a range of applications and properties that entice both chemists and industry professionals.

1. Chemical Structure and Functionality

This compound possesses a unique structure that allows it to exhibit both ionic and covalent characteristics. The presence of an aniline group contributes to its reactivity and versatility:

  • Aromatic Character: The aniline component introduces aromaticity, which can influence the compound's interactions and behavior in reactions.
  • Quaternary Ammonium Nature: As a quaternary ammonium salt, it carries a positive charge, enhancing its solubility in water and ability to engage with various biological systems.

2. Applications in Various Fields

The versatility of this compound makes it valuable in numerous fields, including:

  • Pharmaceuticals: Often utilized in drug formulations and as a therapeutic agent due to its biological properties.
  • Chemical Synthesis: Serves as an intermediate for creating more complex chemical structures.
  • Material Science: Its role in producing functional materials has garnered attention, particularly in coatings and polymers.

3. Biological Relevance

One of the compelling aspects of (2-anilino-2-oxo-ethyl)-diethyl-ammonium;chloride is its interaction with biological systems. Research studies have indicated:

  • Antimicrobial Properties: The compound exhibits properties that may lend it use in combating bacterial infections.
  • Potential Drug Carrier: It has been evaluated as a drug delivery system due to its ionic nature and ability to encapsulate other substances.

4. Synthetic Pathways

The synthesis of this compound involves several steps, often employing traditional organic chemistry techniques. These pathways highlight the compound’s:

  • Reactivity: As an electrophile, it can undergo nucleophilic substitutions.
  • Functionalization: Opportunities to modify and enhance its properties for specific applications.

Conclusion

In summary, (2-anilino-2-oxo-ethyl)-diethyl-ammonium;chloride is more than just a chemical compound; it represents a crossroads of biology, chemistry, and materials science. Its unique properties and wide-ranging applications make it a compelling subject of study for chemists looking to innovate in various domains.

Synonyms
(Diethylamino)acylanilide hydrochloride
IEM-187
3213-15-8
2-(Diethylamino)acetanilide hydrochloride
S 200
W 15565
Acetamide, 2-(diethylamino)-N-phenyl-, hydrochloride
ACETANILIDE, 2-(DIETHYLAMINO)-, HYDROCHLORIDE