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2,3-Dimethoxybuta-1,3-diene

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Identification
Molecular formula
C6H10O2
CAS number
27649-54-1
IUPAC name
2,3-dimethoxybuta-1,3-diene
State
State

At room temperature, 2,3-Dimethoxybuta-1,3-diene is in a liquid state. It is characterized by its fluidity and ability to evaporate quickly compared to more viscous or less volatile compounds.

Melting point (Celsius)
-41.00
Melting point (Kelvin)
232.15
Boiling point (Celsius)
131.50
Boiling point (Kelvin)
404.65
General information
Molecular weight
114.15g/mol
Molar mass
114.1450g/mol
Density
0.8690g/cm3
Appearence

2,3-Dimethoxybuta-1,3-diene is typically a colorless liquid. Its appearance does not change significantly under normal conditions, and it is known for its relatively low viscosity and high volatility.

Comment on solubility

Solubility of 2,3-Dimethoxybuta-1,3-diene

2,3-Dimethoxybuta-1,3-diene, also known as a diene compound, exhibits specific solubility characteristics that can significantly influence its application in various fields. When evaluating the solubility of this compound, several factors come into play:

  • Polar vs Non-Polar Solvents: 2,3-Dimethoxybuta-1,3-diene has two methoxy groups (-OCH3) which introduce some polarity. This leads to the observation that it is more soluble in polar solvents like water or alcohols compared to non-polar solvents.
  • Temperature Dependency: The solubility of the compound may increase with temperature. As with many organic compounds, higher temperatures often facilitate better solvation of molecules.
  • Concentration Considerations: Solubility may also depend on concentration; at higher concentrations, the likelihood of intermolecular interactions increases which may affect solubility.
  • Hydrogen Bonding: The presence of methoxy groups allows for potential hydrogen bonding with water molecules, enhancing solubility in aqueous solutions.

In summary, the solubility of 2,3-dimethoxybuta-1,3-diene is influenced by its molecular structure and the nature of the solvent used. It is essential to conduct experimental assessments for accurate solubility data in varying conditions and solvents.

Interesting facts

Interesting Facts about 2,3-Dimethoxybuta-1,3-diene

2,3-Dimethoxybuta-1,3-diene is an intriguing organic compound that piques the interest of chemists and researchers alike. Here are some fascinating aspects of this compound:

  • Structure and Isomerism: This compound features a unique structure, characterized by the presence of two methoxy groups and a diene system. Its structure allows for different isomers, which can have significant implications in reactivity and properties.
  • Reactivity: The diene component of 2,3-dimethoxybuta-1,3-diene makes it an excellent candidate for various chemical reactions, including Diels-Alder reactions, where it can act as a diene in forming cyclohexene derivatives.
  • Synthetic Utility: Chemists often explore compounds like 2,3-dimethoxybuta-1,3-diene for their potential in synthesizing more complex molecules. Its methoxy substituents can further engage in additional reactions, offering routes to functionalized products.
  • Biological Relevance: While specific biological activities of 2,3-dimethoxybuta-1,3-diene may not be extensively researched, compounds with similar structures have shown potential in pharmaceuticals, possibly acting as precursors to biologically active substances.
  • Historical Context: The study of diene compounds dates back to the early 20th century, when scientists began to explore their properties and applications, paving the way for modern organic chemistry.

In conclusion, 2,3-dimethoxybuta-1,3-diene is not just a simple compound; it embodies a myriad of possibilities in synthetic chemistry and biological applications. As researchers continue to explore its potential, the compound represents an exciting facet of organic chemistry that showcases the intricate relationship between structure and functionality.

Synonyms
2,3-DIMETHOXY-1,3-BUTADIENE
3588-31-6
DTXSID30189438
DTXCID60111929
626-576-9
nhbdkdzhqkqptf-uhfffaoysa-n
2,3-dimethoxybuta-1,3-diene
1,3-Butadiene, 2,3-dimethoxy-
SCHEMBL1721841
2,3-Dimethoxy-buta-1,3-diene
BCP33972
AKOS015912437
2,3-Dimethoxy-1,3-butadiene, 95%
EN300-85834
G77336