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2-Chloro-4,6-diethyl-1,3,5-triazine

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Identification
Molecular formula
C7H11ClN3
CAS number
26182-31-0
IUPAC name
2-chloro-4,6-diethyl-1,3,5-triazine
State
State

At room temperature, 2-Chloro-4,6-diethyl-1,3,5-triazine exists as a liquid.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
171.65g/mol
Molar mass
171.6500g/mol
Density
1.0740g/cm3
Appearence

2-Chloro-4,6-diethyl-1,3,5-triazine is typically a colorless to pale yellow liquid. Its consistency is often described as viscous, and it may be slightly oily to the touch.

Comment on solubility

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

The solubility of 2-chloro-4,6-diethyl-1,3,5-triazine in various solvents can be influenced by its unique molecular structure and functional groups. Typically, this compound exhibits:

  • Limited Water Solubility: As a triazine derivative, it tends to be less soluble in water due to its hydrophobic ethyl groups.
  • Better Solubility in Organic Solvents: It is likely to dissolve more readily in organic solvents such as ethanol, acetone, or chloroform because of its non-polar components.
  • Temperature Effects: The solubility can increase with temperature, making it easier to dissolve in warmth due to enhanced molecular motion.

It's important to note that the solubility of this compound can affect its applications, particularly in agricultural chemistry and other fields where uniform dispersal in a solvent is critical. As such, understanding the solubility characteristics is vital for effective use.

In summary, the solubility behavior of 2-chloro-4,6-diethyl-1,3,5-triazine highlights the significance of solvent choice and environmental conditions for practical applications.

Interesting facts

Interesting Facts about 2-chloro-4,6-diethyl-1,3,5-triazine

2-chloro-4,6-diethyl-1,3,5-triazine is an intriguing nitrogen-containing heterocyclic compound that has garnered interest in various fields of chemistry. Here are some fascinating insights:

  • Structure: This compound features a unique triazine ring, which consists of three nitrogen atoms in a six-membered ring. This notable structure imparts distinctive chemical properties useful in different applications.
  • Reactivity: The presence of the chlorine substituent in its structure increases the reactivity of the molecule, making it a valuable intermediate in organic synthesis, particularly in the development of agrochemicals and pharmaceuticals.
  • Agrochemical Applications: Many triazine derivatives are widely used as herbicides due to their effectiveness in inhibiting plant growth. While 2-chloro-4,6-diethyl-1,3,5-triazine itself may not be a commonly used herbicide, its derivatives can often be found in formulations to control various crops.
  • Synthesis: The synthesis of this compound can be achieved through various methods, including nucleophilic substitution reactions. These pathways often highlight the importance of understanding mechanistic chemistry.
  • Environmental Impact: Like many compounds in the triazine family, environmental scientists are interested in the fate of this compound in the environment, particularly regarding its persistence and potential ecological effects.

The exploration of compounds like 2-chloro-4,6-diethyl-1,3,5-triazine not only enriches our understanding of organic chemistry but also exemplifies the significance of nitrogen-rich compounds in today's scientific landscape. As noted by chemists, "In the realm of organic synthesis, the unique properties of triazines present limitless possibilities."

Synonyms
2-chloro-4,6-diethyl-1,3,5-triazine
701-77-9
SCHEMBL7400206
DB-192603