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Hepta-1,6-dien-4-ol

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Identification
Molecular formula
C7H12O
CAS number
26952-21-6
IUPAC name
hepta-1,6-dien-4-ol
State
State

At room temperature, hepta-1,6-dien-4-ol is in a liquid state.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
174.50
Boiling point (Kelvin)
447.65
General information
Molecular weight
112.17g/mol
Molar mass
112.1740g/mol
Density
0.8425g/cm3
Appearence

Hepta-1,6-dien-4-ol is typically a colorless liquid. Its appearance can be described as clear and has a pungent odor characteristic of alcohols.

Comment on solubility

Solubility of Hepta-1,6-dien-4-ol

Hepta-1,6-dien-4-ol, with its distinctive structure featuring multiple double bonds and a hydroxyl group, presents interesting solubility characteristics. In general, the solubility of a compound is heavily influenced by the following factors:

  • Polarity: Hepta-1,6-dien-4-ol is a polar molecule due to the presence of the hydroxyl (-OH) group, allowing it to engage in hydrogen bonding with water molecules, thereby enhancing its solubility in polar solvents.
  • Structure: The alkene nature of the compound may introduce some hydrophobic characteristics due to the carbon chains, which can limit its solubility in water but improve solubility in organic solvents.
  • Hydrogen Bonding: The hydroxyl group contributes significantly to solubility in polar solvents, making hepta-1,6-dien-4-ol more soluble in alcohols and some aqueous solutions than in purely non-polar solvents.

As a result, while hepta-1,6-dien-4-ol is reasonably soluble in water, it shows a tendency to dissolve better in organic solvents like ethanol or acetone. It’s essential to consider these interactions when studying its chemical properties and applications!

Interesting facts

Interesting Facts about Hepta-1,6-dien-4-ol

Hepta-1,6-dien-4-ol is a fascinating compound that falls under the category of natural products, often showcasing the diversity of organic chemistry. Its structure reveals a unique framework that contributes to various chemical behaviors and applications.

Key Features

  • Structural Complexity: This compound has two double bonds and a hydroxyl group, making it an important subject of study in organic synthesis.
  • Natural Occurrence: Hepta-1,6-dien-4-ol is often found in nature, particularly in plant oils and extracts, highlighting its significance in natural product chemistry.
  • Reactivity: The presence of both double bonds and a hydroxyl group allows for a range of chemical reactivity, such as acting as a nucleophile in various reactions.
  • Flavors and Fragrances: Due to its chemical properties, hepta-1,6-dien-4-ol is investigated for potential use in food flavoring and perfumes.

Applications and Implications

Beyond its structural attributes, hepta-1,6-dien-4-ol holds relevance in various scientific fields:

  • Organic Synthesis: As a versatile starting material, it's used in the creation of more complex molecules.
  • Biological Research: Researchers explore its effects on biological systems, particularly in understanding plant defense mechanisms and metabolic pathways.
  • Material Science: The compound's properties are analyzed for potential applications in developing new materials or polymers.

In summary, hepta-1,6-dien-4-ol is not just an organic compound; it's a bridge connecting various scientific realms—from organic chemistry and natural products to material science and beyond. As scientists continue to uncover its secrets, the possibilities for new discoveries and applications are endless.

Synonyms
Hepta-1,6-dien-4-ol
1,6-HEPTADIEN-4-OL
AI3-37263
EINECS 220-742-0
NSC 97509
BRN 1736942
DTXSID70870999
4-01-00-02249 (Beilstein Handbook Reference)
Hepta1,6dien4ol
DTXCID30818675
220-742-0
2883-45-6
1,6-Heptadiene-4-ol
MFCD00008663
VD28S33WW8
NSC-97509
diallylcarbinol
NSC97509
UNII-VD28S33WW8
SCHEMBL347521
1,6-Heptadien-4-ol, 97%
CHEBI:229301
BBL104178
STL557992
AKOS005259695
MS-20807
SY045301
DB-068013
CS-0064549
NS00048790
EN300-187657