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Identification
Molecular formula
C21H26ClNO4
CAS number
123441-03-2
IUPAC name
diethyl-[3-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxypropyl]ammonium;chloride
State
State

At room temperature, diethyl-[3-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxypropyl]ammonium chloride is in a solid state, generally found in powdered form.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
400.92g/mol
Molar mass
400.9220g/mol
Density
1.3400g/cm3
Appearence

Diethyl-[3-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxypropyl]ammonium chloride typically appears as a crystalline powder. It is known for its white to off-white appearance.

Comment on solubility

Solubility of diethyl-[3-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxypropyl]ammonium;chloride

The solubility of diethyl-[3-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxypropyl]ammonium chloride is influenced by various factors, including its ionic characteristics and polar components. Here are some key points regarding its solubility:

  • Polarity: As a quaternary ammonium salt, this compound exhibits significant polar characteristics, which can lead to high solubility in polar solvents.
  • Solvent Compatibility: It is generally more soluble in water and other polar solvents compared to nonpolar solvents.
  • Ionization: The chloride ion plays a crucial role in enhancing the solubility of the compound in aqueous solutions.
  • Temperature Sensitivity: Like many salts, its solubility may increase with temperature, allowing for better dissolution in hot solvents.

To sum up, the solubility of this compound can be described as favorable in environments that support ion-dipole interactions. Understanding these factors is essential when considering its applications and behavior in various chemical settings.

Interesting facts

Diethyl-[3-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxypropyl]ammonium;chloride

This fascinating compound, often associated with advanced organic synthesis and medicinal chemistry, showcases the complex interplay between structure and functionality. Here are some intriguing facts about it:

  • Unique Structure: The compound features a diethylammonium group that contributes to its properties, which makes it a versatile intermediate in organic reactions.
  • Chromene Core: The presence of a chromene structure in the compound provides interesting optical properties, potentially making it useful in developing fluorescent materials or dyes.
  • Biological Relevance: Compounds with similar structures have been investigated for their potential pharmacological activities, particularly in anti-inflammatory and anti-cancer treatments.
  • Ion Pair Stability: Being a quaternary ammonium salt, the chloride anion enhances the solubility in aqueous environments, thus increasing the bioavailability for potential therapeutic applications.
  • Synthetic Versatility: The compound's synthesis often involves multistep reactions, making it an excellent example for students learning about synthetic techniques in organic chemistry.

As researchers delve into the properties of diethyl-[3-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxypropyl]ammonium;chloride, they continue to uncover its potential uses in various fields. For example, the investigation of its anti-cancer properties might lead to new treatment pathways. The complexity of the molecule also serves to illustrate how slight modifications in chemical structures can lead to vastly different properties and biological activities.

In the words of one prominent chemist, "Understanding the nuances of chemical compounds opens doors to innovations that can change the world."

Thus, diethyl-[3-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxypropyl]ammonium;chloride not only captures the imagination with its intricate structure but also exemplifies the possibilities that lie within the realm of organic chemistry.

Synonyms
3468-08-4
4H-1-Benzopyran-8-carboxylic acid, 3-methyl-4-oxo-2-phenyl-, 3-(diethylamino)propyl ester, hydrochloride
REC 1-0473