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Methybromide

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Identification
Molecular formula
C19H28N2O3Cl
CAS number
847981-70-6
IUPAC name
diethyl-[2-(5-methoxy-1,2-dimethyl-indole-3-carbonyl)oxyethyl]ammonium;chloride
State
State

At room temperature, diethyl-[2-(5-methoxy-1,2-dimethyl-indole-3-carbonyl)oxyethyl]ammonium chloride is in a solid state. This state is typical for ionic compounds, which often form crystalline solids.

Melting point (Celsius)
85.00
Melting point (Kelvin)
358.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
354.88g/mol
Molar mass
354.8810g/mol
Density
1.1200g/cm3
Appearence

The compound diethyl-[2-(5-methoxy-1,2-dimethyl-indole-3-carbonyl)oxyethyl]ammonium chloride is typically a crystalline solid. It appears as a white to off-white powder, indicating its purity and suitability for various applications where coloration could interfere with use.

Comment on solubility

Solubility of Diethyl-[2-(5-methoxy-1,2-dimethyl-indole-3-carbonyl)oxyethyl]ammonium Chloride

The solubility of the compound diethyl-[2-(5-methoxy-1,2-dimethyl-indole-3-carbonyl)oxyethyl]ammonium chloride is influenced by its structure and functional groups. Here are some key points to consider:

  • Polarity: This compound possesses polar functional groups, which generally enhance its solubility in polar solvents such as water.
  • Ionic Interaction: The presence of the chloride ion suggests that the compound is ionic, and ionic compounds typically exhibit higher solubility in solvents with similar polarity.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules can significantly increase solubility; thus, the functional groups may facilitate this.
  • Solvent Choice: It is likely to be more soluble in organic solvents like ethanol or acetone compared to nonpolar solvents due to interactions with the methoxy groups present.
  • Concentration Effects: As with many ionic compounds, its solubility can also vary with temperature; generally, increased temperature may lead to enhanced solubility.

In summary, diethyl-[2-(5-methoxy-1,2-dimethyl-indole-3-carbonyl)oxyethyl]ammonium chloride is expected to be soluble in polar solvents, making it useful in various chemical applications. However, exact solubility data would require experimental validation to determine its behavior in different environments.

Interesting facts

Interesting Facts about Diethyl-[2-(5-Methoxy-1,2-dimethyl-indole-3-carbonyl)oxyethyl]ammonium Chloride

This compound, known for its unique structure and intriguing properties, bears a significant importance in various fields of study, particularly in medicinal chemistry and pharmacology. Here are some engaging insights about this fascinating compound:

  • Origin: Excitingly, this compound is derived from the indole structure, which is a key component in many biologically active compounds, including neurotransmitters and alkaloids.
  • Biological Applications: Compounds related to indole have been known to exhibit a variety of biological activities. This specific compound may play a role in drug development, especially in discovering treatments that leverage its unique properties.
  • Structure-Activity Relationship: The presence of the diethylammonium group and the methoxy- and carbonyl-substituted indole moiety suggests that modifications in the molecular structure can lead to significant variations in biological activity, which is a vital concept in medicinal chemistry.
  • Research Potential: Researchers are continuously exploring the pharmacological effects of compounds similar to this one, particularly their potential as therapeutic agents. The ongoing study in this area can lead to innovative solutions in treating diseases.
  • Chemical Behavior: As a quaternary ammonium compound, it may exhibit interesting properties such as antimicrobial activity, which is highly valuable in developing antiseptic agents or preservatives.

In summary, diethyl-[2-(5-methoxy-1,2-dimethyl-indole-3-carbonyl)oxyethyl]ammonium chloride is more than just a chemical compound; it represents a promising avenue for research that could lead to novel therapies and breakthroughs in our understanding of molecular interactions in biological systems.

Synonyms
18394-54-2
Indole-3-carboxylic acid, 1,2-dimethyl-5-methoxy-, 2-(diethylamino)ethyl ester, monohydrochloride
diethyl-[2-(5-methoxy-1,2-dimethylindole-3-carbonyl)oxyethyl]azanium;chloride
Of-2435