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2,3-Diaminobut-2-enedinitrile

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Identification
Molecular formula
C4H6N4
CAS number
2588-77-2
IUPAC name
2,3-diaminobut-2-enedinitrile
State
State

At room temperature, 2,3-diaminobut-2-enedinitrile exists as a solid. It has a crystalline structure and maintains its form unless exposed to significant changes in temperature or other physical conditions.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.15
Boiling point (Celsius)
274.20
Boiling point (Kelvin)
547.35
General information
Molecular weight
108.12g/mol
Molar mass
108.1170g/mol
Density
1.1440g/cm3
Appearence

2,3-Diaminobut-2-enedinitrile appears as a crystalline solid at room temperature. Its color can range from white to off-white, depending on its purity. The compound is generally stable under normal conditions.

Comment on solubility

Solubility of 2,3-diaminobut-2-enedinitrile

The solubility of 2,3-diaminobut-2-enedinitrile presents interesting characteristics influenced by its chemical structure. This organic compound, with the chemical formula C4H6N4, showcases the following solubility traits:

  • Polar Nature: Due to the presence of multiple amine groups (-NH2) and cyano groups (-C≡N), the compound demonstrates a degree of polarity, which can enhance its interaction with polar solvents.
  • Solvent Compatibility: It tends to be soluble in water and other polar solvents, making it accessible for various applications. However, it might be less soluble in nonpolar solvents.
  • Concentration Effect: At higher concentrations, solubility may change significantly due to factors like solute-solute interactions or precipitation of more complex structures.

In summary, the solubility of 2,3-diaminobut-2-enedinitrile is primarily dictated by its functional groups and the medium in which it is placed. Understanding the specific solubility characteristics can be crucial for its practical applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about 2,3-Diaminobut-2-enedinitrile

2,3-Diaminobut-2-enedinitrile is a fascinating compound in the field of organic chemistry, known for its unique structure and significant applications. Here are some intriguing highlights:

  • Structural Features: The compound features a dinitrile functional group, which makes it highly reactive. This structural aspect contributes to its utility in various synthetic pathways.
  • Biological Interest: 2,3-Diaminobut-2-enedinitrile has garnered attention for its potential biological applications. Research has indicated that derivatives of this compound may exhibit interesting pharmacological activities.
  • Synthetic Utility: This compound serves as an important intermediate in the synthesis of various organic compounds. Its versatility allows chemists to explore multiple reactions, including cyclization and condensation.
  • Importance in Material Science: Due to its nitrogen-rich structure, 2,3-diaminobut-2-enedinitrile is being studied for its potential in developing new materials, including polymers that could have exceptional thermal stability and mechanical properties.
  • Chemical Reactions: The reactivity of the nitrile groups allows for a variety of chemical transformations, making it a valuable building block in the synthesis of heterocycles and other complex organic molecules.

The exploration of 2,3-diaminobut-2-enedinitrile continues to reveal new avenues for research. As scientists delve deeper into its properties and reactions, we remain excited about the potential discoveries this compound holds in both synthesis and application.

Synonyms
diaminobut-2-enedinitrile
DAMN;Hydrogen cyanide tetramer
DPZSNGJNFHWQDC-UHFFFAOYSA-N
AKOS025243518
SB75373
FD183997
DB-025749
DB-041420