Skip to main content

Fenpropimorph

ADVERTISEMENT
Identification
Molecular formula
C19H27NO3S
CAS number
67564-91-4
IUPAC name
[(1S,2R)-2-phenylcyclopropyl]ammonium;[(1R,2S)-2-phenylcyclopropyl]ammonium;sulfate
State
State

At room temperature, this compound is typically in a solid state. Depending on humidity and temperature, it may sometimes appear as a powdery solid.

Melting point (Celsius)
74.00
Melting point (Kelvin)
347.00
Boiling point (Celsius)
348.00
Boiling point (Kelvin)
621.00
General information
Molecular weight
303.43g/mol
Molar mass
303.4260g/mol
Density
1.6800g/cm3
Appearence

The compound generally appears as a white crystalline powder. Its purity and crystal structure can influence its appearance ranging from fine powder to larger crystals.

Comment on solubility

Solubility of [(1S,2R)-2-phenylcyclopropyl]ammonium;[(1R,2S)-2-phenylcyclopropyl]ammonium; sulfate

The solubility of [(1S,2R)-2-phenylcyclopropyl]ammonium;[(1R,2S)-2-phenylcyclopropyl]ammonium; sulfate can be complex due to its unique structural and chemical characteristics. As a quaternary ammonium sulfate, this compound generally exhibits the following traits in terms of solubility:

  • Water Solubility: Quaternary ammonium salts, including this compound, are often highly soluble in water, making them suitable for various applications in aqueous environments.
  • Ionization: The presence of the sulfate ion (SO42-) contributes to solubility, as sulfate salts usually dissolve well in water.
  • Temperature Dependency: Like many chemical compounds, the solubility might increase with temperature, indicating that higher heat can enhance the dissolution process.

In an enriching environment, these compounds can interact in ways that influence their solubility. For example:

  • In the presence of organic solvents, solubility may vary significantly.
  • pH levels can also play a crucial role; certain ionic compounds might become less soluble at extreme pH values.

In summary, the solubility of [(1S,2R)-2-phenylcyclopropyl]ammonium;[(1R,2S)-2-phenylcyclopropyl]ammonium; sulfate is generally favorable in water due to its ionic nature, though specific conditions must be considered for complete solubility assessment. This compound embodies important characteristics of quaternary ammonium compounds that are essential for their functional application in chemical processes.

Interesting facts

Interesting Facts about [(1S,2R)-2-phenylcyclopropyl]ammonium;[(1R,2S)-2-phenylcyclopropyl]ammonium; sulfate

This compound, a fascinating example of chiral ammonium salts, showcases the intriguing world of stereochemistry and its applications in pharmaceutical research. The presence of the cyclopropyl and phenyl groups gives it unique reactivity and potential biological properties. Here are some interesting aspects:

  • Chirality: The compound contains two chiral centers, making it exist as two enantiomers: (1S,2R) and (1R,2S). This is significant in pharmacology, as the different enantiomers may exhibit different biological activities.
  • Pharmaceutical Potential: Compounds like this one are being explored for their potential use in medicinal chemistry, particularly for their effects on neurological pathways, due to their unique structural features that may influence receptor interactions.
  • Sulfate Component: The sulfate ion contributes to the overall stability and solubility of the salt, and it also plays a role in biological systems, functioning as a signaling molecule.
  • Synthetic Applications: The preparation of such ammonium salts involves chiral synthesis techniques, which highlight the advancements in organic synthesis, allowing chemists to produce enantiomerically pure compounds.

As stated by renowned chemist Linus Pauling, "If you want to be a chemist, you must be prepared to think about things differently." This compound serves as an excellent example of how molecular structure can variably influence chemical functionality and interaction. The study of such compounds continues to be a pivotal area of research in chemistry and biochemistry.