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2,4,6-Tris(3-nitrophenyl)-1,3,5-triazine

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Identification
Molecular formula
C21H12N6O6
CAS number
65182-90-3
IUPAC name
2,4,6-tris(3-nitrophenyl)-1,3,5-triazine
State
State

This compound is a solid at room temperature.

Melting point (Celsius)
263.00
Melting point (Kelvin)
536.15
Boiling point (Celsius)
486.00
Boiling point (Kelvin)
759.15
General information
Molecular weight
447.36g/mol
Molar mass
447.3500g/mol
Density
1.3540g/cm3
Appearence

2,4,6-Tris(3-nitrophenyl)-1,3,5-triazine typically appears as a crystalline solid. The compound is often yellow due to the presence of nitro groups, which contribute to its characteristic color.

Comment on solubility

Solubility of 2,4,6-tris(3-nitrophenyl)-1,3,5-triazine

The solubility of 2,4,6-tris(3-nitrophenyl)-1,3,5-triazine can be quite intriguing due to its complex molecular structure and the nature of the functional groups present. As a triazine derivative, this compound exhibits some notable characteristics regarding its solubility in different solvents.

Solubility Characteristics

  • The compound is usually considered to be sparingly soluble in water due to its extensive aromatic character and the presence of nitro groups which can influence its polarity.
  • It tends to dissolve better in organic solvents that can accommodate its hydrophobic structures, such as dimethyl sulfoxide (DMSO) or acetone.
  • This limited solubility in water can be attributed to the need for strong interactions to overcome the hydrophobic effects present in its triazine and phenyl groups.

In conclusion, understanding the solubility behavior of 2,4,6-tris(3-nitrophenyl)-1,3,5-triazine is essential when considering its application in various chemical processes. The predominant organic solvent solubility could play a key role in its functionality and use in different formulations.

Interesting facts

Interesting Facts about 2,4,6-tris(3-nitrophenyl)-1,3,5-triazine

2,4,6-tris(3-nitrophenyl)-1,3,5-triazine is a fascinating compound notable for its unique structure and diverse applications. Here are some key insights:

  • Versatile Applications: This compound is often used in the fields of chemistry and material sciences, particularly as a dye or pigment due to its vivid color properties. Its high stability and lightfastness make it ideal for use in various coatings and textiles.
  • Biological Significance: Interestingly, compounds similar to this triazine derivative have been investigated for their potential as herbicides and pesticides. The triazine ring is known for its effectiveness in inhibiting photosynthesis in some plants, showcasing a dual-use scenario in scientific research.
  • Synthetic Pathways: The synthesis of 2,4,6-tris(3-nitrophenyl)-1,3,5-triazine involves reactions that often require advanced techniques. Researchers frequently explore various reaction conditions to optimize yield while ensuring both safety and environmental considerations are met.
  • Colorimetry: This compound is utilized in colorimetric analysis, where it serves as a reagent for detecting specific ions or molecules. Its ability to change color in response to chemical reactions allows for simpler visual assessments in laboratories.
  • Research and Innovation: As a chemist or an enthusiastic student, exploring the compound's properties can lead to innovative applications in organic electronics, as researchers are continuously investigating new materials for use in components like OLEDs (Organic Light Emitting Diodes).

A compound of this nature not only represents a plethora of chemical properties but also embodies the ongoing pursuit of knowledge and discovery within the scientific community. As you delve deeper into its characteristics, you may find exciting new avenues for research or practical applications that could benefit society.

Synonyms
2,4,6-tris(3-nitrophenyl)-1,3,5-triazine
DTXSID30274813
14043-38-0
DTXCID30226271