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Identification
Molecular formula
C12H20INO2
CAS number
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IUPAC name
[(2R,3R)-3-hydroxy-2-methyl-2,3-dihydrobenzofuran-7-yl]-trimethyl-ammonium;iodide
State
State

The compound is generally in a solid state at room temperature.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.00
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.00
General information
Molecular weight
273.21g/mol
Molar mass
273.2060g/mol
Density
1.3204g/cm3
Appearence

The compound is typically a white solid, with no distinct odor. It is usually available in crystalline form and slightly hygroscopic in nature.

Comment on solubility

Solubility of [(2R,3R)-3-hydroxy-2-methyl-2,3-dihydrobenzofuran-7-yl]-trimethyl-ammonium;iodide

The compound [(2R,3R)-3-hydroxy-2-methyl-2,3-dihydrobenzofuran-7-yl]-trimethyl-ammonium;iodide exhibits interesting solubility characteristics that can be summarized as follows:

  • Water Solubility: The quaternary ammonium structure generally enhances solubility in polar solvents such as water due to the presence of charged ammonium groups.
  • Solvent Versatility: It may also be soluble in a variety of organic solvents. Solubility can be influenced by factors like solvent polarity and temperature.
  • Ion Pairing: The iodide counterion may contribute to its solubility behavior, especially in mixed solvent systems. An increase in ion pairing can often lead to enhanced solubility in polar solvents.

In general, charged species like this compound tend to have better solubility profiles in polar environments, while their behavior in nonpolar solvents might be limited. Understanding the solubility of such compounds is crucial for applications in fields such as pharmaceuticals and materials science.

Therefore, it is recommended to perform specific solubility tests to determine its behavior under various conditions, keeping in mind that temperature and pH can play significant roles in the solubility of this compound.

Interesting facts

Interesting Facts About [(2R,3R)-3-hydroxy-2-methyl-2,3-dihydrobenzofuran-7-yl]-trimethyl-ammonium;iodide

This compound, known for its quaternary ammonium structure, has garnered attention in various realms of chemistry and medicinal research. Let's explore some key aspects:

  • Quaternary Ammonium Compound: As a quaternary ammonium compound, it can act as a surfactant and plays a role in pharmaceuticals due to its ability to interact with biological membranes.
  • Medicinal Potential: The unique structure of this compound makes it a subject of interest in drug development. Its derivatives may exhibit various biological activities, potentially contributing to therapeutic solutions.
  • Chirality: The presence of chirality at the 2R and 3R positions indicates that it can exist in different enantiomers, which can lead to different physiological effects in biological systems.
  • Functional Group Diversity: The hydroxyl group present in the structure enhances its reactivity, allowing it to participate in multiple chemical reactions, such as esterifications or nucleophilic substitutions.
  • Structural Beauty: With its dihydrobenzofuran framework, the compound offers insight into the fascinating world of heterocycles, showcasing how they contribute to the complexity and richness of organic compounds.

Overall, this compound illustrates the interplay between chemical structure and biological function, showcasing the importance of detailed molecular understanding in enhancing the efficacy of therapeutic agents.

Synonyms
26819-65-8
DTXSID80949620
3-Hydroxy-N,N,N,2-tetramethyl-2,3-dihydro-1-benzofuran-7-aminium iodide
RefChem:1067980
DTXCID401377804
cis-(2,3-Dihydro-3-hydroxy-2-methyl-7-benzofuranyl)trimethylammonium iodide
Ammonium, (2,3-dihydro-3-hydroxy-2-methyl-7-benzofuranyl)trimethyl-, (Z)-, iodide