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Camphoric acid

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Identification
Molecular formula
C10H16O2
CAS number
464-49-3
IUPAC name
6,7,7-trimethyltricyclo[6.2.1.01,5]undec-5-ene-2-carboxylic acid
State
State

At room temperature, camphoric acid is in a crystalline solid state. It is typically found as a white powder.

Melting point (Celsius)
187.00
Melting point (Kelvin)
460.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
168.21g/mol
Molar mass
168.2100g/mol
Density
1.1425g/cm3
Appearence

Camphoric acid typically appears as colorless or white crystalline powder. It does not have a strong or distinctive odor.

Comment on solubility

Solubility of 6,7,7-trimethyltricyclo[6.2.1.01,5]undec-5-ene-2-carboxylic acid

The solubility of 6,7,7-trimethyltricyclo[6.2.1.01,5]undec-5-ene-2-carboxylic acid can be described as intriguing due to its unique structure and functional groups. Here are some key points to consider:

  • Polar vs. Non-Polar: This compound contains a carboxylic acid group which tends to increase the polarity, enhancing its potential to dissolve in polar solvents like water.
  • Hydrophobic Regions: With a complex tricyclic structure, parts of the molecule may exhibit hydrophobic characteristics, making it less soluble in water.
  • Solubility in Organic Solvents: It often displays greater solubility in organic solvents such as acetone or ethanol, aligning with many organic compounds that share similar structural features.
  • Temperature Dependence: Like many compounds, its solubility is likely temperature-dependent, often increasing at higher temperatures.

In summary, the solubility of 6,7,7-trimethyltricyclo[6.2.1.01,5]undec-5-ene-2-carboxylic acid is a variable trait influenced by its molecular characteristics and the nature of the solvent employed. Exploring this compound in various solvents can reveal fascinating insights into its behavior in solution.

Interesting facts

Interesting Facts about 6,7,7-Trimethyltricyclo[6.2.1.01,5]undec-5-ene-2-carboxylic Acid

6,7,7-Trimethyltricyclo[6.2.1.01,5]undec-5-ene-2-carboxylic acid is a fascinating compound that falls under the category of carboxylic acids, known for their unique structural features and reactivity. Here are some key points that highlight the characteristics and significance of this compound:

  • Complex Structure: The compound belongs to a class of tricyclic structures, characterized by three interconnected rings. The intricate arrangement contributes to its unique chemical behavior.
  • Natural Occurrence: Tricyclic compounds, including this acid, can often be found in various natural products, including certain plant metabolites, which makes them of interest in natural product chemistry.
  • Potential Applications: Owing to its unique structure, this compound may have potential applications in fields such as medicine and agriculture, particularly in the design of novel pharmaceuticals or agrochemicals.
  • Reactivity: The carboxylic acid functional group in this compound typically exhibits various reactivity patterns, enabling it to participate in multiple chemical reactions, such as esterification and amide formation.
  • Research Interest: Scientists are intrigued by its properties which may provide insights into stereochemistry and molecular interactions, enriching the understanding of molecular design.

As you dive into the study of 6,7,7-trimethyltricyclo[6.2.1.01,5]undec-5-ene-2-carboxylic acid, keep in mind that compounds like this one reveal the intricate tapestry of chemistry and its potential to influence various industries!

Synonyms
ISOZIZANOIC ACID
16202-79-2
Isokhusenic acid
DTXSID30936626
1H-3a,6-Methanoazulene-3-carboxylic acid, 2,3,4,5,6,7-hexahydro-7,7,8-trimethyl-, [3S-(3.alpha.,3a.alpha.,6.alpha.)]-
1H-3a.alpha.,6-Methanoazulene-3-carboxylic acid, 2,3.beta.,4,5,6.beta.,7-hexahydro-7,7,8-trimethyl-
6,7,7-Trimethyl-tricyclo[6.2.1.01,5 ]undec-5-en-2-yl carboxylic acid
7,7,8-trimethyl-2,3,4,5,6,7-hexahydro-1H-3a,6-methanoazulene-3-carboxylic acid
(3S,3aS,6R)-7,7,8-Trimethyl-2,3,4,5,6,7-hexahydro-1H-3a,6-methanoazulene-3-carboxylic acid
1H-3a,6-Methanoazulene-3-carboxylic acid, 2,3,4,5,6,7-hexahydro-7,7,8-trimethyl-, (3S,3aS,6R)-