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2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide

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Identification
Molecular formula
C12H8N2O2
CAS number
61132-54-3
IUPAC name
2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide
State
State

This compound is generally found as a solid at room temperature.

Melting point (Celsius)
37.00
Melting point (Kelvin)
310.15
Boiling point (Celsius)
190.30
Boiling point (Kelvin)
463.45
General information
Molecular weight
196.20g/mol
Molar mass
146.2190g/mol
Density
1.0650g/cm3
Appearence

2,4,6-Trimethylbenzene-1,3-dicarbonitrile oxide appears as a crystalline solid, typically in the form of white crystals or powder.

Comment on solubility

Solubility of 2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide

The solubility of 2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide (C12H8N2O2) presents several interesting aspects:

  • Polarity: The presence of hydroxyl (–OH) functionality typically increases solubility in polar solvents, while nonpolar hydrocarbon chains can favor solubility in nonpolar solvents.
  • Solvent Interactions: This compound may exhibit greater solubility in organic solvents such as ethanol or acetone, which can interact favorably with the nitrogen and oxygen atoms present.
  • Temperature Dependence: Solubility can also be influenced by temperature; increased temperatures often lead to higher solubility for many organic compounds.

Notably, 2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide may show limited solubility in water due to its hydrophobic aromatic structure:

  • Hydrophobic Character: The bulky aromatic system reduces the overall interaction with water molecules.
  • Complexity of Structure: The combination of multiple functional groups may create a balance that influences overall solubility behavior.

To summarize, the solubility of 2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide is dictated by its unique molecular structure, solvent choice, and environmental conditions. Its behavior underscores the intricate relationship between molecular configuration and solubility potential.

Interesting facts

Interesting Facts about 2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide

2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide, often simply referred to as a complex organic compound, has piqued the interest of chemists due to its intriguing structure and potential applications. Here are some fascinating points about this compound:

  • Unique Structure: The compound features a benzene ring substituted with three methyl groups and two functional nitrile oxide groups. This creates a structure that is highly specific and demonstrates the rich chemistry of substituted aromatic compounds.
  • Versatile Reactivity: Nitrile oxides are known for their reactivity, particularly in forming isocyano compounds and their potential in cycloaddition reactions, which can lead to the synthesis of more complex molecules.
  • Potential Applications: Due to its unique functional groups, this compound may find applications in fields such as:
    • Organic synthesis
    • Material science
    • Pharmaceutical development
  • Environmental Implications: Compounds with nitrile groups are often studied for their environmental impact and degradation pathways, making this compound a candidate for investigation regarding ecological safety.
  • Chemical Toolbox: The presence of the dicarbonitrile oxide group allows for various synthetic pathways that are useful for chemists looking to design new materials or explore unusual chemical reactions.

In conclusion, 2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide represents a fascinating intersection of structure, reactivity, and potential applications, making it a compound of interest in both academic research and industrial chemistry.

Synonyms
15138-43-9
2,4,6-trimethylbenzene-1,3-dicarbonitrile oxide
ISOPHTHALONITRILE, 2,4,6-TRIMETHYL-, N,N'-DIOXIDE
2,4,6-Trimethyl-1,3-benzenedicarbonitrile oxide
NSC 93008
BRN 3096014
2,4,6-Trimethylisophthalonitrile N,N'-dioxide
NSC93008
1,3-Benzenedicarbonitrile, 2,4,6-trimethyl-, N,N'-dioxide
DTXSID40164771
NSC-93008
1, 2,4,6-trimethyl-, N,N'-dioxide
2,6-Trimethylisophthalonitrile N,N'-dioxide
Isophthalonitrile,4,6-trimethyl-, N,N'-dioxide