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3,4-Dimethylhex-3-en-2-one

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Identification
Molecular formula
C8H14O
CAS number
81788-24-9
IUPAC name
3,4-dimethylhex-3-en-2-one
State
State

At room temperature, 3,4-Dimethylhex-3-en-2-one is in a liquid state.

Melting point (Celsius)
-65.00
Melting point (Kelvin)
208.15
Boiling point (Celsius)
137.00
Boiling point (Kelvin)
410.15
General information
Molecular weight
126.20g/mol
Molar mass
126.1960g/mol
Density
0.8073g/cm3
Appearence

3,4-Dimethylhex-3-en-2-one is a colorless liquid. It has a clear appearance with no solid components.

Comment on solubility

Solubility of 3,4-Dimethylhex-3-en-2-one

3,4-Dimethylhex-3-en-2-one, a compound with the formula C9H16O, showcases interesting solubility characteristics. Being an organic compound, its solubility is greatly influenced by its molecular structure and the presence of functional groups.

Key points about the solubility of 3,4-dimethylhex-3-en-2-one include:

  • Solvent Compatibility: This compound is generally soluble in organic solvents such as ethanol, ether, and acetone due to its nonpolar and slightly polar regions.
  • Water Solubility: Due to its molecular structure, which lacks significant polar functional groups, 3,4-dimethylhex-3-en-2-one is expected to have low solubility in water. This is typical of compounds that do not participate in strong hydrogen bonding with water molecules.
  • Temperature Effect: Like many organic compounds, its solubility may change with temperature; higher temperatures typically enhance solubility in nonpolar solvents.

In conclusion, while the compound is readily soluble in nonpolar and some polar organic solvents, it is practically insoluble in water, highlighting the classic behavior of similar organic molecules.

Interesting facts

Interesting Facts about 3,4-Dimethylhex-3-en-2-one

3,4-Dimethylhex-3-en-2-one, also known as a type of enone, presents a fascinating structure that has garnered attention in organic chemistry due to its unique properties and reactivity. Here are some intriguing facts about this compound:

  • Structure and Isomerism: This compound features a double bond in its chain, which adds to its structural complexity. The presence of two methyl groups at the 3 and 4 positions plays a significant role in its chemical behavior and stability.
  • Chemical Reactivity: As a conjugated enone, the compound exhibits *interesting reactivity patterns*, including Michael addition reactions and enolate formation, making it a versatile intermediate in organic synthesis.
  • Biological Activity: Compounds within the enone family have been studied for their potential biological activities. They may exhibit various pharmacological effects, attracting attention for further research in medicinal chemistry.
  • Synthetic Applications: Due to its structure, 3,4-dimethylhex-3-en-2-one can serve as a building block for the synthesis of more complex molecules, especially in the fields of natural product synthesis and material science.

As chemists continue to explore the vast realm of organic compounds, 3,4-dimethylhex-3-en-2-one stands out as a noteworthy example of how simple modifications in molecular structure can lead to diverse reactivity and applications. Its study can further enhance our understanding of enone chemistry, leading to innovative developments in various scientific fields.

Synonyms
1635-02-5
3,4-Dimethyl-3-hexen-2-one
RefChem:271178
3-Hexen-2-one, 3,4-dimethyl-, (E)-
3,4-dimethyl 3-hexen 2-one
SCHEMBL8651598
WRHRFVOAEDXVPC-UHFFFAOYSA-N
DTXSID201030882
NS00048509