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2,6-dimethyloct-2-ene

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Identification
Molecular formula
C10H20
CAS number
4930-99-0
IUPAC name
2,6-dimethyloct-2-ene
State
State

At room temperature, 2,6-dimethyloct-2-ene is in the liquid state.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
143.00
Boiling point (Kelvin)
416.15
General information
Molecular weight
126.24g/mol
Molar mass
126.2390g/mol
Density
0.7320g/cm3
Appearence

2,6-Dimethyloct-2-ene typically appears as a colorless liquid. It does not exhibit any significant color and is mainly used in chemical research and industrial applications.

Comment on solubility

Solubility of 2,6-Dimethyloct-2-ene

2,6-Dimethyloct-2-ene, with the molecular formula C10H18, is an organic compound primarily recognized for its properties as an alkene. When discussing the solubility of this compound, it is essential to consider several key factors:

  • Hydrophobicity: Due to its long hydrophobic carbon chain, 2,6-dimethyloct-2-ene exhibits low solubility in polar solvents such as water.
  • Apolar Solvents: It is, however, more soluble in non-polar solvents like hexane or petroleum ether. The lack of functional groups increases its compatibility with apolar environments.
  • Temperature Effects: Like many organic compounds, solubility can increase with temperature, promoting interactions in non-polar solvents.

In summary, while 2,6-dimethyloct-2-ene is poorly soluble in water, its solubility in non-polar organic solvents makes it a useful compound in organic chemistry applications. As always, solubility properties should be evaluated in the context of the intended chemical reactions or processes.

Interesting facts

Interesting Facts about 2,6-Dimethyloct-2-ene

2,6-Dimethyloct-2-ene is an intriguing organic compound belonging to the alkene family, characterized by its double bond and branched structure. Here are some captivating aspects of this compound:

  • Structure and Isomerism: This compound features a unique structure with two methyl groups attached to the second and sixth carbon atoms of the octene chain. This branching leads to interesting geometric isomerism, where the positioning of the double bond can create different visual orientations.
  • Applications: Alkene compounds like 2,6-dimethyloct-2-ene are often used in the production of various polymers and plastics. Their ability to undergo reactions—such as polymerization—makes them significant in chemical manufacturing.
  • Reactivity: Due to the presence of a double bond, 2,6-dimethyloct-2-ene exhibits higher reactivity compared to alkanes. It can undergo several reactions, including hydrogenation, halogenation, and hydroboration-oxidation, which are essential for synthetic organic chemistry.
  • Environmental Considerations: Understanding compounds like 2,6-dimethyloct-2-ene is fundamental in the study of environmental chemistry. Alkenes can contribute to photochemical smog formation, highlighting the importance of balancing their industrial utility with environmental impact.
  • Natural Occurrence: Many alkenes, including those structurally similar to 2,6-dimethyloct-2-ene, can be found in nature, particularly in essential oils and natural plant products, showcasing their biological relevance.

In conclusion, 2,6-dimethyloct-2-ene is more than just a chemical; it represents a key nexus between structure, reactivity, and real-world applications, making it a fascinating topic for both budding chemists and seasoned professionals.

Synonyms
2,6-Dimethyl-2-octene
2-OCTENE, 2,6-DIMETHYL-
2,6-Dimethyl-oct-2-ene
NSC 91458
BRN 1719569
3-01-00-00861 (Beilstein Handbook Reference)
wqnlwkdarwvske-uhfffaoysa-n
2,6-dimethyloct-2-ene
4057-42-5
2-Octene,6-dimethyl-
NCIOpen2_001334
DTXSID80871053
NSC91458
LMFA11000593
NSC-91458
AKOS006277366