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1,6-Heptadiene

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Identification
Molecular formula
C7H12
CAS number
592-83-6
IUPAC name
hepta-1,6-diene
State
State
At room temperature, 1,6-Heptadiene is a liquid.
Melting point (Celsius)
-119.00
Melting point (Kelvin)
154.15
Boiling point (Celsius)
98.40
Boiling point (Kelvin)
371.55
General information
Molecular weight
96.17g/mol
Molar mass
96.1700g/mol
Density
0.7100g/cm3
Appearence

1,6-Heptadiene is a colorless liquid with a characteristic odor. It is known for its simplicity in structure as a linear alkene hydrocarbon containing two double bonds.

Comment on solubility

Solubility of Hepta-1,6-diene

Hepta-1,6-diene, with the chemical formula C7H12, exhibits interesting solubility properties primarily due to its hydrocarbon nature. Being an alkene, this compound features multiple double bonds which influence its interactions with solvents.

When discussing solubility, several key aspects come into play:

  • Polar vs. Nonpolar Solvents: Hepta-1,6-diene is nonpolar, making it more soluble in nonpolar solvents such as hexane, toluene, and other hydrocarbons.
  • Solubility in Water: This compound is expected to be insoluble in water due to the significant polarity difference between water and the nonpolar hepta-1,6-diene.
  • Temperature Dependency: As with many organic compounds, solubility can be influenced by temperature; higher temperatures may enhance solubility in nonpolar organic solvents.

To summarize, it can be stated that:

  • Hepta-1,6-diene is best dissolved in nonpolar solvents.
  • It shows minimal solubility in polar solvents like water.

Understanding these solubility dynamics is essential for applications and reactions involving hepta-1,6-diene, contributing to its overall utility in chemical processes.

Interesting facts

Interesting Facts About Hepta-1,6-diene

Hepta-1,6-diene is a fascinating compound within the realm of organic chemistry. This compound is particularly noteworthy for its unique structure and properties. Here are some intriguing points about hepta-1,6-diene:

  • Unsaturated Nature: Hepta-1,6-diene contains two double bonds, making it a diene. These double bonds play a crucial role in its reactivity and ability to participate in various chemical reactions.
  • Applications in Synthesis: Due to its unsaturated bonds, hepta-1,6-diene serves as an important intermediate in organic synthesis. It can be utilized in producing larger molecules in fields like pharmaceuticals and polymer chemistry.
  • Isomeric Forms: This diene can exist in different isomeric forms. The arrangement of carbon atoms and the location of double bonds can lead to several structural variations, impacting its chemical behavior and reactivity.
  • Chemical Reactions: Hepta-1,6-diene participates in various reactions, including electrophilic addition and polymerization. This makes it a valuable compound for chemists looking to create new materials or compounds.
  • Study of Stability: Scientists study the stability of hepta-1,6-diene and similar compounds to understand the factors that influence the stability of unsaturated hydrocarbons. Factors such as steric strain and substitution can significantly affect their chemical properties.
  • Cosmetic and Fragrance Industry: The unique scent profile of certain hydrocarbons, including derivatives of hepta-1,6-diene, has caught the attention of perfumers. They explore its potential use in creating novel fragrances.

In summary, hepta-1,6-diene is not just a simple molecule; it holds significant importance in the fields of organic chemistry and industry. Its fascinating structural characteristics and reactivity make it a subject of ongoing research and interest.

Synonyms
1,6-HEPTADIENE
3070-53-9
CH2=CH(CH2)3CH=CH2
DTXSID2062828
DTXCID1038244
626-010-0
geawfzntifjmhr-uhfffaoysa-n
Hepta-1,6-diene
MFCD00008667
1,6-Heptadiene, 99%
BCP23784
AKOS025295109
H0564
T72268
Q19833899