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2-chloro-4-ethyl-6-phenyl-1,3,5-triazine

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Identification
Molecular formula
C11H10ClN3
CAS number
1070-14-8
IUPAC name
2-chloro-4-ethyl-6-phenyl-1,3,5-triazine
State
State

At room temperature, 2-chloro-4-ethyl-6-phenyl-1,3,5-triazine is typically found in a solid state, appearing as crystalline powder.

Melting point (Celsius)
69.00
Melting point (Kelvin)
342.15
Boiling point (Celsius)
303.00
Boiling point (Kelvin)
576.15
General information
Molecular weight
217.66g/mol
Molar mass
217.6610g/mol
Density
1.1850g/cm3
Appearence

2-Chloro-4-ethyl-6-phenyl-1,3,5-triazine typically appears as a white to off-white crystalline powder, showcasing the characteristic structural motifs of triazines with substituted phenyl and ethyl groups that may slightly alter its color and texture.

Comment on solubility

Solubility of 2-chloro-4-ethyl-6-phenyl-1,3,5-triazine

The solubility of 2-chloro-4-ethyl-6-phenyl-1,3,5-triazine can be described as generally low in water, primarily due to its hydrophobic aromatic and alkyl groups. However, when considering its solubility in organic solvents, the characteristics shift considerably:

  • Organic solvents: This compound readily dissolves in a range of organic solvents such as ethyl acetate, acetone, and chloroform.
  • Water: Due to its relatively large molecular structure, the compound has limited solubility in water, often quantified in parts per million (ppm), and generally characterized as being non-polar.

Factors influencing solubility include:

  1. Molecular structure: The presence of multiple aromatic rings contributes to lower water solubility.
  2. Temperature: Increased temperatures can enhance solubility in organic solvents.
  3. pH of the solution: Although this compound does not possess acidic or basic functional groups, the medium's characteristics can affect dissolution behavior.

In summary, 2-chloro-4-ethyl-6-phenyl-1,3,5-triazine exhibits selective solubility, being more compatible with organic solvents than with water, highlighting the significance of solvent choice in practical applications.

Interesting facts

Interesting Facts about 2-Chloro-4-ethyl-6-phenyl-1,3,5-triazine

2-Chloro-4-ethyl-6-phenyl-1,3,5-triazine is a fascinating compound with applications across various fields. Here are some key points that highlight its significance:

  • Versatile Applications: This compound has garnered attention in the realm of agricultural chemistry, primarily as an effective herbicide, helping in weed control in various crops.
  • Synthesis Pathways: The synthesis of triazine derivatives is of great interest in organic chemistry. This compound can be synthesized through nucleophilic substitution reactions, showcasing the importance of reaction mechanisms in forming new compounds.
  • Heterocyclic Chemistry: The triazine ring itself is a notable feature, comprising three nitrogen atoms in a six-membered aromatic structure. This highlights its role in heterocyclic chemistry, where compounds with nitrogen-containing rings demonstrate unique reactivity and properties.
  • Biological Activity: Studies have indicated that triazine derivatives can exhibit biological activities, making them potential candidates for further drug development. The ongoing research explores their interaction with biological systems, which may lead to novel therapeutic agents.
  • Environmental Impact: Given its use as a herbicide, understanding the environmental persistence and degradation pathways of 2-chloro-4-ethyl-6-phenyl-1,3,5-triazine is crucial. Research in this area contributes to greater ecological safety and sustainable agricultural practices.

In conclusion, 2-chloro-4-ethyl-6-phenyl-1,3,5-triazine serves as a significant example of how chemical compounds can bridge the gap between theoretical chemistry and practical applications. As scientists continue to explore its properties, we may uncover even more exciting uses and characteristics in the future.

Synonyms
2-chloro-4-ethyl-6-phenyl-1,3,5-triazine
13704-97-7
DTXSID40274804
DTXCID40226262
SCHEMBL7523521