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3-dodec-2-enyltetrahydrofuran-2,5-dione

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Identification
Molecular formula
C16H24O3
CAS number
72356-00-4
IUPAC name
3-dodec-2-enyltetrahydrofuran-2,5-dione
State
State

At room temperature, 3-dodec-2-enyltetrahydrofuran-2,5-dione is typically a liquid. It is not commonly found as a solid due to its relatively low melting point.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.15
Boiling point (Celsius)
326.00
Boiling point (Kelvin)
599.15
General information
Molecular weight
268.41g/mol
Molar mass
268.4070g/mol
Density
0.9230g/cm3
Appearence

3-Dodec-2-enyltetrahydrofuran-2,5-dione appears as a light yellow to pale brown liquid. It has a characteristic odor often associated with ketones and esters.

Comment on solubility

Solubility of 3-Dodec-2-enyltetrahydrofuran-2,5-dione

The solubility of 3-dodec-2-enyltetrahydrofuran-2,5-dione can be explored through several key points:

  • Polarity: The presence of polar functional groups in the compound suggests that it may exhibit moderate solubility in polar solvents.
  • Hydrophobic Chain: The long hydrophobic dodec-2-enyl chain may lead to limited solubility in water, promoting solubility in non-polar organic solvents.
  • Temperature Effects: Like many organic compounds, solubility may increase with temperature, making it more soluble in heated organic solvents.
  • Common Solvents: Likely soluble in solvents such as ethanol, chloroform, or acetone due to their non-polar to slightly polar nature.

In summary, while 3-dodec-2-enyltetrahydrofuran-2,5-dione may have a complex solubility profile influenced by both its polar and non-polar characteristics, it is generally expected to be poorly soluble in water but more soluble in organic solvents. Understanding these solubility characteristics can help in applications such as formulation and synthesis.

Interesting facts

Exploring 3-Dodec-2-enyltetrahydrofuran-2,5-dione

3-Dodec-2-enyltetrahydrofuran-2,5-dione is a fascinating chemical compound that draws attention for several reasons. Here are some intriguing insights:

  • Structural Complexity: This compound features a unique four-membered tetrahydrofuran ring, which adds to its chemical resilience and diversity in reactivity.
  • Natural Occurrence: Compounds similar to 3-Dodec-2-enyltetrahydrofuran-2,5-dione can be isolated from various natural sources, hinting at its biological significance.
  • Synthetic Applications: Its structural motif is important in organic synthesis, particularly in the design of pharmaceuticals and agrochemicals, due to its ability to facilitate reactions.
  • Versatile Functional Groups: The presence of dione groups in the structure enhances its ability to undergo different chemical transformations, making it a key player in synthetic chemistry.

“The universe is under no obligation to make sense to you.” – Neil deGrasse Tyson
This quote resonates with scientists as they explore the intricacies of chemical compounds like 3-Dodec-2-enyltetrahydrofuran-2,5-dione, where each reaction or product can lead to unexpected discoveries.

Moreover, understanding such compounds could lead to advancements in:

  1. Medicinal Chemistry: Discovering new therapeutic agents.
  2. Material Science: Developing innovative materials with unique properties.
  3. Environmental Chemistry: Studying its role and degradation in ecological systems.

In conclusion, 3-Dodec-2-enyltetrahydrofuran-2,5-dione exemplifies the interplay of structure and function in organic chemistry, offering an array of research avenues and applications that can significantly impact various fields.

Synonyms
(2-Dodecen-1-yl)succinic anhydride
2-Dodecen-1-ylsuccinic anhydride
3-(2-dodecenyl)dihydro-2,5-furandione
Dodecenyl succinic anhydride
2-DODECENYL SUCCINIC ANHYDRIDE
SUCCINIC ANHYDRIDE, (2-DODECENYL)-
RefChem:471336
3-dodec-2-enyloxolane-2,5-dione
2-Dodecenylsuccinic anhydride
SCHEMBL714069
HMS3755G05
3-dodec-2-enyltetrahydrofuran-2,5-dione
(2-Dodecen-1-yl)succinic anhydride, 95%
NS00010064
(2-Dodecen-1-yl)succinic anhydride, technical
E78826
(2-Dodecen-1-yl)succinic anhydride, ~95% (titration)