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Furtrethonium acetate

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Identification
Molecular formula
C17H22NO2.C2H4O2
CAS number
64-46-8
IUPAC name
2-furylmethyl-(1-methyl-2-phenyl-ethyl)ammonium;acetate
State
State

This compound is a solid at room temperature. It is stable and retains its solid form unless subjected to temperatures above its melting point.

Melting point (Celsius)
128.00
Melting point (Kelvin)
401.00
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.00
General information
Molecular weight
277.35g/mol
Molar mass
277.3450g/mol
Density
1.1403g/cm3
Appearence

Furtrethonium acetate typically appears as a white crystalline solid. This detailed solid form makes it easy to identify and store. Its crystalline nature provides an indication of high purity, which is crucial for chemical applications.

Comment on solubility

Solubility of 2-furylmethyl-(1-methyl-2-phenyl-ethyl)ammonium;acetate

The solubility of 2-furylmethyl-(1-methyl-2-phenyl-ethyl)ammonium acetate can be influenced by various factors, including the compound's ionic character and molecular structure. Here are some key points to consider:

  • Ionic Nature: Being a salt, 2-furylmethyl-(1-methyl-2-phenyl-ethyl)ammonium acetate is expected to be soluble in polar solvents.
  • Solvent Interaction: Its solubility may increase significantly in water due to the formation of favorable hydrogen bonds between the solvent and the ammonium group.
  • Temperature Dependency: Generally, as temperature increases, the solubility of salts in water also increases. This could lead to enhanced solubility of the compound at elevated temperatures.
  • Organic Solvents: The presence of aromatic rings suggests potential compatibility with some non-polar or slightly polar organic solvents, although solubility can vary based on the specific solvent.

In summary, while 2-furylmethyl-(1-methyl-2-phenyl-ethyl)ammonium acetate is likely to have reasonable solubility in water, the precise solubility profile would require experimental determination to account for all contributing factors.

Interesting facts

Interesting Facts about 2-furylmethyl-(1-methyl-2-phenyl-ethyl)ammonium Acetate

The compound known as 2-furylmethyl-(1-methyl-2-phenyl-ethyl)ammonium acetate is fascinating due to its unique molecular structure and functional properties. Here are several key points to consider:

  • Structural Diversity: This compound features a combination of a furan ring and an ammonium group, showcasing the beauty of organic synthesis. The furan moiety is known for its aromaticity and reactivity, which makes it a valuable segment in pharmaceuticals.
  • Pharmacological Relevance: Compounds containing ammonium groups are often investigated for their biological activities. This particular compound may exhibit interesting pharmacological properties, thus enticing medicinal chemists for further study.
  • Ion-Pair Formation: The presence of an acetate counterion indicates that the compound could participate in ion-pair formation, which is crucial for enhancing solubility in various solvents and could impact its biochemical interactions.
  • Chirality: The presence of a chiral center in the 1-methyl-2-phenyl-ethyl moiety implies that this compound may exist in enantiomeric forms. Chirality in pharmaceuticals can significantly influence their efficacy and safety profiles, pointing to the importance of stereoisomerism in drug design.
  • Potential Applications: Given its structural characteristics, this compound may be explored for various applications, including as a ligand in coordination chemistry, or as a precursor in the synthesis of more complex organic compounds.

In summary, 2-furylmethyl-(1-methyl-2-phenyl-ethyl)ammonium acetate is more than just a chemical compound; it represents a nexus of chemistry and potential applications in the realms of pharmaceutical and materials science. Researchers are constantly seeking innovative ways to utilize its unique features in advancing both basic and applied sciences.

Synonyms
N-(alpha-Methylphenethyl)furfurylamine acetate
2980-12-3
FURFURYLAMINE, N-(alpha-METHYLPHENETHYL)-, ACETATE (+-)-