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Identification
Molecular formula
C34H62ClNO2
CAS number
2367743-94-6
IUPAC name
(2-tert-butoxy-2-oxo-ethyl)-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State
At room temperature, this compound is typically in a solid state. It can be characterized by its crystalline structure and white appearance. It is generally stable under standard conditions but should be stored in a dry environment to avoid moisture absorption.
Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.00
General information
Molecular weight
357.93g/mol
Molar mass
357.9270g/mol
Density
1.0331g/cm3
Appearence

The compound appears as a white or off-white crystalline solid. The crystals may vary in size and shape, often appearing as fine powder or small crystalline chunks. It may also come in a semi-amorphous form and can demonstrate slight hygroscopic properties, absorbing moisture from the air to some extent.

Comment on solubility

Solubility of (2-tert-butoxy-2-oxo-ethyl)-(1,7,7-trimethylnorbornan-2-yl)ammonium; chloride

The solubility of this compound can be quite interesting due to its dual nature as an ammonium salt. Ammonium compounds often exhibit specific solubility characteristics based on their structural components. Here are some key points to consider:

  • Water Solubility: As a chloride salt, it is likely to be soluble in water, as most organic ammonium chlorides dissolve well in aqueous solutions.
  • Solvent Interaction: The presence of the tert-butoxy group suggests that there may be a moderate to high solubility in organic solvents such as ethanol or acetone, making it versatile in various chemical environments.
  • Temperature Dependency: Solubility can be affected by temperature, where increasing temperature may enhance solubility in both water and organic solvents.
  • pH Influence: Changes in pH can also affect the solubility characteristics of this compound, particularly as an ammonium salt, where higher acidity could lead to increased solubility.

Overall, the solubility profile of (2-tert-butoxy-2-oxo-ethyl)-(1,7,7-trimethylnorbornan-2-yl)ammonium; chloride reflects its unique chemical structure and functional groups, making it a subject of interest in both aqueous and non-aqueous systems.

Interesting facts

Interesting Facts about (2-tert-butoxy-2-oxo-ethyl)-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride

This compound is a remarkable example of a quaternary ammonium salt, which is a significant class of compounds in the realm of organic chemistry. Quaternary ammonium compounds are known for their diverse applications due to their surfactant properties, as well as their utility in the fields of biochemistry and pharmacology.

Structural Insights

  • The compound contains a tert-butoxy group that contributes to its steric bulk and lipophilicity.
  • Its norbornane structure can be attributed to the cyclic nature that imparts stability and unique reactivity patterns, making it interesting for synthetic applications.
  • The quaternary nitrogen atom signifies that this compound is positively charged, providing potential for electrostatic interactions in biological systems.

Applications and Significance

  • Surface Active Agent: Due to its amphiphilic nature, this compound can function effectively as a surfactant, helping to lower surface tension in various applications.
  • Biological Activity: Quaternary ammonium compounds can exhibit antimicrobial properties, potentially making this compound relevant in the development of disinfectants and antiseptics.
  • Chemical Reactions: The presence of the carbonyl group in the structure can open pathways for further chemical reactions, useful in synthesis and functionalization.

It's fascinating to consider how the unique structural features of this compound can translate into specific activities within biological systems and industrial applications. As researchers continue to explore and understand such complex compounds, we can expect new and innovative uses to emerge, revealing the versatility and importance of quaternary ammonium salts in modern chemistry.

Synonyms
(+-)-endo-N-2-Bornylglycine tert-butyl ester hydrochloride
24629-61-6
GLYCINE, N-2-BORNYL-, tert-BUTYL ESTER, HYDROCHLORIDE, endo-(+-)-
RefChem:346541