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Camphor

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Identification
Molecular formula
C10H16O
CAS number
76-22-2
IUPAC name
1,3,3,7-tetramethylnorbornan-2-one
State
State

At room temperature, camphor is a solid. It sublimes easily, transitioning from a solid to a gas without passing through a liquid phase.

Melting point (Celsius)
175.00
Melting point (Kelvin)
448.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.15
General information
Molecular weight
152.24g/mol
Molar mass
152.2370g/mol
Density
0.9920g/cm3
Appearence

Camphor is a waxy, white or transparent solid with a strong, aromatic odor. Its crystalline structure can give it a shiny appearance.

Comment on solubility

Solubility of 1,3,3,7-tetramethylnorbornan-2-one

The solubility of 1,3,3,7-tetramethylnorbornan-2-one can be quite intriguing, primarily because of its unique structural characteristics. As an organic compound, its solubility is influenced by factors such as polarity, molecular weight, and interactions with solvents.

Key Points on Solubility:

  • Polarity: The presence of the carbonyl group (C=O) suggests that this compound may exhibit some polar characteristics, potentially allowing for solubility in polar solvents.
  • Hydrophobic Regions: The bulky non-polar portions of the molecule, particularly due to the numerous methyl groups, generally increase hydrophobic interactions, making it less soluble in water.
  • Common Solvents: You might find that 1,3,3,7-tetramethylnorbornan-2-one is more soluble in organic solvents such as dichloromethane or ethyl acetate due to its organic nature.
  • Temperature Influence: Like most organic compounds, the solubility can also increase with temperature, which may facilitate the dissolution process in suitable solvents.

In summary, while 1,3,3,7-tetramethylnorbornan-2-one has potential solubility in various solvents, its overall solubility profile is complex and heavily influenced by its molecular structure and the nature of the solvent.

Interesting facts

Interesting Facts about 1,3,3,7-Tetramethylnorbornan-2-one

1,3,3,7-Tetramethylnorbornan-2-one is a fascinating compound in the field of organic chemistry, especially for its unique structural characteristics and potential applications. Here are some intriguing aspects of this compound:

  • Structural Beauty: The molecule is a derivative of norbornane, showcasing a bicyclic structure that is both robust and versatile. The presence of four methyl groups at positions 1, 3, and 7 adds to its complexity and interesting sterics.
  • Synthesis Potential: This compound can be synthesized through various methods, including the photochemical degradation of derivatives or through multi-step synthetic pathways. Its synthesis provides ample opportunities for students to explore advanced organic reactions.
  • Applications: 1,3,3,7-Tetramethylnorbornan-2-one is of interest in the synthesis of other organic compounds, potentially serving as a building block in the pharmaceutical and agrochemical industries.
  • Chirality and Isomerism: The unique arrangement of its substituents offers a rich discussion on chirality and stereochemistry, making it an excellent study case for students interested in these concepts.
  • Intriguing Reactivity: As a ketone, its chemical reactivity is quite interesting, allowing for various reactions including nucleophilic additions. This makes it a subject of interest for research in reaction mechanisms.

Through its structural features, synthetic pathways, and applications, 1,3,3,7-tetramethylnorbornan-2-one embodies the intersection of science and creativity, inspiring new ideas and developments in the chemical world. As a compound with multiple potential applications, it certainly deserves a prominent place in the study of organic chemistry.

Synonyms
15404-57-6
1,3,3,7-TETRAMETHYL-2-OXOBICYCLO(2.2.1)HEPTANE
1,3,3,7-TETRAMETHYLBICYCLO[2.2.1]HEPTAN-2-ONE
DTXSID70934904