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Tropone

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Identification
Molecular formula
C7H6O
CAS number
539-80-0
IUPAC name
cyclohepta-2,4,6-trien-1-one
State
State

At room temperature, tropone is typically a yellow crystalline solid, which sublimates easily.

Melting point (Celsius)
29.00
Melting point (Kelvin)
302.15
Boiling point (Celsius)
117.00
Boiling point (Kelvin)
390.15
General information
Molecular weight
92.10g/mol
Molar mass
92.1020g/mol
Density
1.1330g/cm3
Appearence

Tropone is a yellow crystalline solid with a distinct aromatic odor.

Comment on solubility

Solubility of Cyclohepta-2,4,6-trien-1-one

Cyclohepta-2,4,6-trien-1-one, with the chemical formula C8H8O, exhibits unique solubility characteristics due to its molecular structure and the presence of a carbonyl (C=O) group. Understanding its solubility helps in various applications and theoretical studies.

Key Points on Solubility:

  • Solvent Compatibility: Cyclohepta-2,4,6-trien-1-one is generally soluble in organic solvents such as ethanol, acetone, and dichloromethane.
  • Polar vs. Nonpolar: The compound's moderate polarity allows it to dissolve better in slightly polar solvents compared to nonpolar solvents.
  • Temperature Influence: Like many organic compounds, its solubility may increase with temperature, facilitating its use in synthetic processes.

In essence, the solubility of cyclohepta-2,4,6-trien-1-one is dictated by its molecular interactions with solvents, making it an interesting compound for further research and practical applications.

Interesting facts

Interesting Facts About Cyclohepta-2,4,6-trien-1-one

Cyclohepta-2,4,6-trien-1-one, often referred to simply as "cycloheptatrienone," is a fascinating compound in the realm of organic chemistry. Here are some intriguing aspects that highlight its significance:

  • Unique Structure: This compound features a cyclic structure that includes both conjugated double bonds and a ketone functional group. The presence of these features contributes to its reactivity and potential applications in organic synthesis.
  • Conjugation Effects: The alternating double bonds provide a level of stability and influence the compound's chemical properties. Conjugation allows for the delocalization of electrons, which can enhance reactivity and stability.
  • Synthetic Interest: Cyclohepta-2,4,6-trien-1-one holds considerable interest for chemists looking to create complex organic molecules. Its reactive nature makes it a valuable intermediate in synthetic pathways.
  • Potential Applications: The compound can serve as a precursor in the synthesis of other organic compounds, including drugs and natural products, showcasing its versatility in medicinal chemistry.
  • Research Focus: Ongoing studies aim to explore the photochemical properties of cycloheptatrienone, which can lead to novel applications, particularly in material science and organic electronics.

In summary, cyclohepta-2,4,6-trien-1-one stands out not only for its intriguing molecular structure but also for its potential contributions to organic synthesis and the development of new materials. Its characteristics embody the beauty and complexity of organic chemistry!

Synonyms
Tropone
cyclohepta-2,4,6-trien-1-one
2,4,6-CYCLOHEPTATRIEN-1-ONE
Cycloheptatrienone
Tropon
2,4,6-Cycloheptatriene-1-one
UNII-CO48X7SUFH
CO48X7SUFH
cyclohepta-2,4,6-trienone
EINECS 208-725-6
2,4,6-cycloheptatrienone
2,4,6-cycloheptatrien-1-on
DTXSID60202169
2,4,6-CYCLOHEPTATRIN-1-ONE
DTXCID10124660
inchi=1/c7h6o/c8-7-5-3-1-2-4-6-7/h1-6
qvwdctqrorvhht-uhfffaoysa-n
539-80-0
MFCD00014331
Tropone, 97%
SCHEMBL316824
SCHEMBL18727723
AKOS024365345
FC59201
HY-W035904
DB-052444
CS-0088241
NS00043109
D74673
Q413630
doi:10.14272/QVWDCTQRORVHHT-UHFFFAOYSA-N.1