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Hex-2-enyl acetate

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Identification
Molecular formula
C8H14O2
CAS number
2497-18-9
IUPAC name
hex-2-enyl acetate
State
State
Hex-2-enyl acetate is a liquid at room temperature.
Melting point (Celsius)
-100.00
Melting point (Kelvin)
173.15
Boiling point (Celsius)
174.00
Boiling point (Kelvin)
447.15
General information
Molecular weight
142.21g/mol
Molar mass
142.2080g/mol
Density
0.8775g/cm3
Appearence

Hex-2-enyl acetate is a colorless liquid with a fruity odor. It is commonly used in flavors and fragrances for its sweet, apple-like scent. The liquid is typically clear and free from suspended matter.

Comment on solubility

Solubility of Hex-2-enyl Acetate

Hex-2-enyl acetate, a compound known for its pleasant fruity aroma, displays interesting solubility characteristics. Overall, the solubility of this compound can be summarized as follows:

  • Polar Solvents: Hex-2-enyl acetate is less soluble in polar solvents due to its non-polar hydrocarbon chain. However, it can exhibit some degree of solubility in light polar solvents.
  • Non-polar Solvents: It shows good solubility in non-polar solvents such as hexane and benzene, attributed to its hydrophobic hydrocarbon structure.
  • Water Solubility: This compound is generally insoluble in water, aligning with the general behavior of esters with longer carbon chains.

In practice, the solubility of hex-2-enyl acetate in various media can be important for its applications, particularly in the flavor and fragrance industries. As stated in literature, "the solubility profile can significantly influence the efficacy of the compound in formulations."

In summary, while hex-2-enyl acetate may not dissolve well in water, its compatibility with non-polar solvents opens the door for diverse applications. Consider these factors when working with this compound.

Interesting facts

Interesting Facts about Hex-2-enyl Acetate

Hex-2-enyl acetate, an intriguing compound in the world of organic chemistry, belongs to the family of esters. It is primarily known for its unique characteristics and applications. Here are some engaging facts about this compound:

  • Aromatic Appeal: Hex-2-enyl acetate possesses a pleasant fruity aroma, which is why it is often utilized in the fragrance and flavoring industries. Its scent profile makes it a popular choice for perfumes.
  • Natural Occurrence: This compound can be found naturally in various fruits, contributing to their delightful fragrances. It is often associated with citrus and tropical scents.
  • Functional Versatility: In addition to its use in fragrances, hex-2-enyl acetate serves as an important intermediate in organic synthesis. It can be transformed into other valuable chemical entities through various reactions, thus playing a crucial role in pharmaceuticals and agrochemicals.
  • Industrial Relevance: The compound is also employed in the production of plastics and synthetic materials, showcasing its versatility in different industrial applications.
  • Reactivity Profile: Hex-2-enyl acetate features a double bond in its structure, which makes it a candidate for various chemical reactions, including polymerization and addition reactions. This reactivity allows chemists to explore diverse pathways for compound manipulation.

In summary, hex-2-enyl acetate is more than just a simple ester; it is a compound filled with both practical and theoretical significance in the realms of organic chemistry, ecology, and industry. Its unique properties not only enhance our sensory experiences but also provide vital pathways for synthetic chemistry.

Synonyms
Hex-2-enyl acetate
2-Hexen-1-ol, acetate, (2E)-
2-Hexen-1-ol, 1-acetate
2-hexen-1-yl acetate
DTXSID90862972
EINECS 233-223-9
DTXCID90811662
10094-40-3
Hex-2-enyl acetate(isomer unspecified)
DB-046596
NS00082535