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Tropinone

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Identification
Molecular formula
C8H13NO
CAS number
532-24-1
IUPAC name
potassium;2-[(1R)-cyclohex-3-en-1-yl]-2-oxo-acetate
State
State

At room temperature, tropinone is typically in a solid state, specifically as a powder.

Melting point (Celsius)
41.00
Melting point (Kelvin)
314.15
Boiling point (Celsius)
197.00
Boiling point (Kelvin)
470.15
General information
Molecular weight
139.19g/mol
Molar mass
139.1880g/mol
Density
1.2205g/cm3
Appearence

Tropinone appears as white to off-white crystalline powder.

Comment on solubility

Solubility of Potassium 2-[(1R)-Cyclohex-3-en-1-yl]-2-oxo-acetate

When considering the solubility of potassium 2-[(1R)-cyclohex-3-en-1-yl]-2-oxo-acetate, several factors come into play:

  • Potassium Salts: Salts containing potassium are generally known for their good solubility in water. They often dissociate readily into their ionic components.
  • Polar Functional Groups: The presence of polar functional groups, such as the ketone and carboxylate moieties in this compound, enhances solubility in polar solvents, particularly water.
  • Organic Solubility: Given the cyclohexenyl group, the compound may also exhibit solubility in organic solvents, especially those like ethanol or acetone, which can facilitate interactions through hydrophobic and Van der Waals forces.

It is crucial to note that while hydroxyl and carboxyl groups promote solubility, the bulkiness introduced by the cyclohexenyl group may hinder it somewhat in certain solvents. Therefore, one might observe:

  1. **High solubility in aqueous solutions** due to potassium ion dissociation and interaction with water.
  2. **Moderate solubility in organic solvents**, dependent on solvent polarity and the compound's hydrophobic characteristics.

In conclusion, while the solubility of potassium 2-[(1R)-cyclohex-3-en-1-yl]-2-oxo-acetate is likely favorable, it can vary significantly based on the solvent environment. Always conduct solubility tests in the specific solvent of interest for precise determinations.

Interesting facts

Exploring 2-[(1R)-cyclohex-3-en-1-yl]-2-oxo-acetate of Potassium

2-[(1R)-cyclohex-3-en-1-yl]-2-oxo-acetate potassium salt, commonly referred to as a potassium compound, belongs to a fascinating class of organic compounds noted for their various applications in chemical synthesis and medicinal chemistry. Here are some engaging highlights about this intriguing compound:

  • Natural Origins: This compound’s structure includes a cyclohexene ring, which is a common feature in many naturally occurring compounds. Its framework often lends itself to complex biological activity, making it a point of interest in natural product chemistry.
  • Reactivity and Synthesis: The presence of the ester functional group and the carbonyl group (oxo) in its structure can make it a versatile intermediate in organic synthesis. Scientists often utilize such compounds for creating more complex molecules through various reactions, including nucleophilic additions and substitutions.
  • Biological Significance: Compounds featuring cyclohexene rings are often studied for their potential biological activities, including anti-inflammatory and anti-cancer properties. This compound may hold promise for medicinal applications that warrant further investigation.
  • Coordination Chemistry: The potassium salt of this compound can act as a source of potassium ions, which are essential for many biological functions and play critical roles in cellular processes, such as nerve impulse transmission and muscle contraction.
  • Application in Agriculture: Salts of organic acids like this compound can also be relevant in agriculture, serving as fertilizers that supply essential nutrients to plants.

As a chemist or student of chemistry, understanding compounds like 2-[(1R)-cyclohex-3-en-1-yl]-2-oxo-acetate potassium opens doors to innovative research and applications in multiple fields, illustrating the intricate links between organic chemistry and real-world applications.