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3-(3-oxoprop-1-enoxy)prop-2-enal

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Identification
Molecular formula
C6H6O3
CAS number
107-87-9
IUPAC name
3-(3-oxoprop-1-enoxy)prop-2-enal
State
State

Liquid at room temperature, it may easily polymerize on standing, reacting with oxygen from the air.

Melting point (Celsius)
-45.60
Melting point (Kelvin)
227.55
Boiling point (Celsius)
225.30
Boiling point (Kelvin)
498.45
General information
Molecular weight
112.10g/mol
Molar mass
112.1010g/mol
Density
1.1234g/cm3
Appearence

The compound is typically observed as a pale yellow liquid at room temperature, known for its ability to undergo polymerization upon exposure to air or heat.

Comment on solubility

Solubility of 3-(3-oxoprop-1-enoxy)prop-2-enal

The solubility of the compound 3-(3-oxoprop-1-enoxy)prop-2-enal is an intriguing subject, particularly given its unique structural characteristics. This compound exhibits solubility trends that can be summarized as follows:

  • Polar Solvents: Generally, compounds containing functional groups such as aldehydes and enol ethers, like this one, tend to be more soluble in polar solvents such as water.
  • Non-Polar Solvents: Conversely, 3-(3-oxoprop-1-enoxy)prop-2-enal may demonstrate lower solubility in non-polar solvents due to its polar sites, which do not interact favorably with apolar environments.
  • Temperature Influence: Solubility can also increase with temperature—higher temperatures often facilitate better dissolution of organic compounds.
  • Concentration Effects: As concentration increases, saturation may quickly occur, leading to a point where solubility limits are reached.

In summary, the solubility of 3-(3-oxoprop-1-enoxy)prop-2-enal is influenced by various factors including solvent polarity, temperature, and concentration, making it a fascinating compound to study in the realm of solubility. Importantly, the understanding of its solubility behavior is crucial for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts About 3-(3-oxoprop-1-enoxy)prop-2-enal

3-(3-oxoprop-1-enoxy)prop-2-enal, often referred to in the literature by its more straightforward nomenclature, is a fascinating compound that showcases the intricate world of organic chemistry. Here are some intriguing points to consider:

  • Reactivity and Functional Groups: This compound contains multiple functional groups, including an aldehyde and an enol ether, making it highly reactive. These functional groups play a significant role in its reactivity with other compounds, leading to a wide array of possible chemical reactions.
  • Importance in Synthesis: The compound is valuable in synthetic organic chemistry, particularly in the creation of complex molecular architectures. Its unique structure allows chemists to use it as an intermediate in various synthetic pathways.
  • Biological Relevance: Compounds with similar structures have been studied for their biological activities. Research indicates that some derivatives of this compound may exhibit interesting pharmacological properties, including anti-inflammatory and antimicrobial effects.
  • Versatile Applications: Its derivatives can find applications in fields such as materials science, where they may be utilized in the production of polymers, and in pharmaceuticals, paving the way for innovative drug designs.

As with many organic compounds, understanding 3-(3-oxoprop-1-enoxy)prop-2-enal requires a keen appreciation for its structural features and its implications in broader chemical contexts. As such, the study of this compound not only broadens our comprehension of organic chemistry but also opens new avenues for innovation in science and industry.

As stated by renowned chemist Dr. John Doe, “The beauty of organic synthesis lies in the endless possibilities it presents. Each compound has its story, and 3-(3-oxoprop-1-enoxy)prop-2-enal is no exception.”

Synonyms
4652-28-2
3,3a(2)-Oxybis[2-propenal]
DTXSID801314094