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Camphor

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Identification
Molecular formula
C10H16O
CAS number
76-22-2
IUPAC name
2,6,6-trimethylnorpinan-3-one
State
State

At room temperature, camphor exists as a solid. It readily sublimes, which means it can transition directly from a solid to a gas at atmospheric pressure, contributing to its distinctive smell.

Melting point (Celsius)
179.00
Melting point (Kelvin)
452.15
Boiling point (Celsius)
209.00
Boiling point (Kelvin)
482.15
General information
Molecular weight
152.24g/mol
Molar mass
152.2370g/mol
Density
0.9900g/cm3
Appearence

Camphor is a white, waxy, crystalline solid with a strong, aromatic odor. It is somewhat translucent, with a glossy surface, and can appear in several forms including tablets, blocks, or powder.

Comment on solubility

Solubility of 2,6,6-trimethylnorpinan-3-one

2,6,6-trimethylnorpinan-3-one, a compound with a complex structure, exhibits unique solubility properties that can be influenced by various factors. Understanding its solubility is crucial for applications in fields like pharmaceuticals and organic synthesis.

Factors Influencing Solubility

  • Polarity: The polarity of the compound plays a significant role in its solubility. Non-polar solvents generally dissolve non-polar compounds better.
  • Temperature: Increased temperatures often enhance solubility due to greater molecular motion.
  • Presence of Functional Groups: The specific functional groups can significantly affect how well the compound interacts with solvents.

In practice, 2,6,6-trimethylnorpinan-3-one may demonstrate varied solubility in different solvents. Typical behaviors can include:

  1. Good solubility in organic solvents: Such as ethanol and dichloromethane, due to similar polarity.
  2. Poor solubility in water: The hydrophobic regions of the molecule tend to resist interaction with water molecules.

In conclusion, the solubility of 2,6,6-trimethylnorpinan-3-one is largely determined by its structural features and the nature of the solvent used. As a result, comprehending these relationships is essential for harnessing the full potential of this compound in various applications.

Interesting facts

Interesting Facts about 2,6,6-Trimethylnorpinan-3-one

2,6,6-trimethylnorpinan-3-one is a fascinating compound that belongs to the class of cyclic ketones. Its unique structure and properties make it noteworthy in various scientific fields.

Chemical Structure and Properties

The compound features a bicyclic structure with multiple methyl groups attached, which significantly influences its chemical characteristics. Here are some points that highlight its structure:

  • Bicyclic Nature: The compound's bicyclic framework contributes to its stability and ability to undergo specific chemical reactions.
  • Methyl Substituents: The presence of three methyl groups enhances steric hindrance, impacting both reactivity and potential interactions with other molecules.

Applications and Significance

This compound holds importance in various fields, including:

  • Synthesis of Natural Products: Its structure can serve as a precursor in synthesizing biologically active compounds.
  • Fragrance Industry: The compound may find use in creating specific scents, thanks to its aromatic properties.

Research Insights

There are ongoing studies exploring the potential of 2,6,6-trimethylnorpinan-3-one, which include:

  • Drug Development: Its structural features are of interest in developing new pharmaceuticals.
  • Cheminformatics: The compound is often analyzed using modern computational techniques to predict its behavior and interactions.

As a scientist or chemistry student, studying 2,6,6-trimethylnorpinan-3-one provides valuable insights into the world of organic chemistry and the intricate relationships between structure and function in chemical compounds. Its unique properties and potential applications make it an exciting subject of research and exploration!

Synonyms
3-Pinanone
Bicyclo[3.1.1]heptan-3-one, 2,6,6-trimethyl-
Bicyclo(3.1.1)heptan-3-one, 2,6,6-trimethyl-
Bicyclo3.1.1heptan-3-one, 2,6,6-trimethyl-
2,6,6-Trimethylbicyclo[3.1.1]heptan-3-one
(E)-Pinocamphone
15358-88-0
(1alpha,2beta,5alpha)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
Bicyclo[3.1.1]heptan-3-one, 2,6,6-trimethyl-, (1.alpha.,2.alpha.,5.alpha.)-
1S,2R,5R-3-Pinanone
D-Pinocamphone
2,6,6-trimethylnorpinan-3-one
pinan-3-one
Pinocamphone, trans
SCHEMBL7839978
DTXSID60862166
CHEBI:171963
AAA47362
MFCD31630144
SY224505
NS00084069
NS00084366
NS00085303
2,7,7-trimethyl-bicyclo[3.1.1]heptan-3-one
2,6,6-Trimethylbicyclo[3.1.1]heptan-3-one, 9CI
Q67865674
2,6,6-Trimethylbicyclo[3.1.1]heptan-3-one, (1.alpha.,2.alpha.,5.alpha.)-