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Triethyl 1,3,5-triazine-2,4,6-tricarboxylate

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Identification
Molecular formula
C12H15N3O6
CAS number
15708-41-5
IUPAC name
triethyl 1,3,5-triazine-2,4,6-tricarboxylate
State
State

At room temperature, triethyl 1,3,5-triazine-2,4,6-tricarboxylate is a solid compound. It is stable under normal conditions and does not easily evaporate or sublimate.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
313.27g/mol
Molar mass
313.2980g/mol
Density
1.3521g/cm3
Appearence

Triethyl 1,3,5-triazine-2,4,6-tricarboxylate is typically a crystalline solid at room temperature. Its appearance is characterized by a white to off-white color, and it usually comes in the form of fine powder or small crystals.

Comment on solubility

Solubility of Triethyl 1,3,5-Triazine-2,4,6-Tricarboxylate

Triethyl 1,3,5-triazine-2,4,6-tricarboxylate, a complex organic compound, exhibits intriguing solubility characteristics. Solubility is influenced by several factors including molecular structure, polarity, and the solvent employed. In particular, the following points are noteworthy:

  • Polarity: Triethyl 1,3,5-triazine-2,4,6-tricarboxylate contains multiple carboxylate groups which contribute to its polarity. This usually enhances solubility in polar solvents such as water.
  • Solvent Interaction: The compound is typically soluble in organic solvents like ethanol and acetone due to its ethyl groups, which can interact favorably with non-polar environments.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature; thus, heating the solvent may assist in dissolving the compound more effectively.

However, it is crucial to note that the actual solubility can vary based on the specific conditions and concentrations involved. As a general guideline, “the solubility of a compound can often be predicted by the 'like dissolves like' principle,” where polar compounds tend to dissolve in polar solvents, and non-polar in non-polar.

In summary, while triethyl 1,3,5-triazine-2,4,6-tricarboxylate is likely to demonstrate reasonable solubility in polar solvents, its behavior in different environments makes it a compound of interest for further exploration.

Interesting facts

Interesting Facts about Triethyl 1,3,5-Triazine-2,4,6-tricarboxylate

Triethyl 1,3,5-triazine-2,4,6-tricarboxylate is a fascinating compound that falls under the category of triazine derivatives. These compounds are known for their diverse applications in various fields, primarily due to their unique chemical structure. Here are some intriguing aspects:

  • Aromatic Characteristics: The triazine ring structure contributes to the compound's ability to participate in pi-stacking interactions, enhancing its reactivity in certain conditions.
  • Biological Activities: Several studies suggest that triazine derivatives possess noteworthy biological properties, potentially serving as antimicrobial or antifungal agents, making them of interest in medicinal chemistry.
  • Industrial Applications: Triethyl 1,3,5-triazine-2,4,6-tricarboxylate is often employed in the synthesis of various agrochemicals, such as herbicides and insecticides, underscoring its importance in agricultural sciences.
  • Environmental Relevance: The compound’s potential role in environmental sustainability is being explored, particularly in the development of biodegradable materials and effective pollution control agents.
  • Versatile Reactivity: The presence of multiple carboxylate groups enhances its reactivity, allowing it to undergo various chemical modifications. This versatility opens doors to introducing new functional groups and designing novel compounds.

The study of triethyl 1,3,5-triazine-2,4,6-tricarboxylate exemplifies the intersection of organic chemistry with applied sciences, highlighting the importance of understanding such compounds for future innovations. As one researcher aptly put it, "Chemistry is a language; every molecule tells a story." Through understanding molecules like this triazine derivative, we begin to narrate our own story of discovery and innovation.

Synonyms
2,4,6-triethyl 1,3,5-triazine-2,4,6-tricarboxylate
844-841-9
Triethyl 1,3,5-triazine-2,4,6-tricarboxylate
898-22-6
C12H15N3O6
2,4,6-Triethoxycarbonyl-1,3,5-triazine
triethyl-1,3,5-triazine-2,4,6-tricarboxylate
MFCD01419268
SCHEMBL352579
CHEMBL4991680
1,3,5-Triazine-2,4,6-tricarboxylic acid, triethyl ester
DTXSID30274530
LKNPNZKIOSOWES-UHFFFAOYSA-N
AAA89822
2,4,6-Triethoxycarbonyl-s-triazine
STK540195
AKOS001325045
SB73709
AS-66462
DB-353156
CS-0204292
EN300-26716
E84637
Triethyl1,3,5-triazine-2,4,6-tricarboxylate
AH-262/34227006
TRIETHYL 1 3 5-TRIAZINE-2 4 6-TRICARBOX&
Triethyl 1,3,5-triazine-2,4,6-tricarboxylate, 97%
Z228460230