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Cloprop

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Identification
Molecular formula
C11H2Cl7N3
CAS number
101-27-9
IUPAC name
2-(2-chlorophenyl)-4,6-bis(trichloromethyl)-1,3,5-triazine
State
State

At room temperature, Cloprop is in a solid state. It remains stable and does not undergo significant changes in appearance when exposed to a range of typical laboratory environmental conditions.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
391.00
Boiling point (Kelvin)
664.15
General information
Molecular weight
406.87g/mol
Molar mass
406.8690g/mol
Density
1.6200g/cm3
Appearence

Cloprop is typically a colorless crystalline solid. It is often observed as a white powder, which may appear slightly off-white due to impurities. The crystal structure makes it distinctly identifiable under a microscope.

Comment on solubility

Solubility of 2-(2-chlorophenyl)-4,6-bis(trichloromethyl)-1,3,5-triazine

The solubility of the compound 2-(2-chlorophenyl)-4,6-bis(trichloromethyl)-1,3,5-triazine, a triazine derivative, can be quite intriguing, given its distinct structural characteristics. This compound exhibits limited solubility in several common solvents, primarily due to its heavily chlorinated structure, which affects its polarity and overall interaction with solvents.

Key points regarding its solubility include:

  • Low Solubility in Water: The compound is generally considered insoluble in water, which is common for many chlorinated organic compounds.
  • Solubility in Organic Solvents: It tends to dissolve in various organic solvents such as dichloromethane, chloroform, and acetonitrile due to their nonpolar characteristics that accommodate the chlorinated regions.
  • Hydrophobic Interactions: The presence of multiple trichloromethyl groups significantly contributes to its hydrophobic nature, leading to a preference for nonpolar environments.

As a conclusion, the solubility behavior of 2-(2-chlorophenyl)-4,6-bis(trichloromethyl)-1,3,5-triazine underscores the significance of molecular structure in determining solubility. Understanding these properties is essential for applications in formulations and environmental science, where solubility plays a critical role.

Interesting facts

Interesting Facts about 2-(2-Chlorophenyl)-4,6-bis(trichloromethyl)-1,3,5-triazine

This compound represents a fascinating class of chemicals known as triazines, which are notable for their diverse applications in agriculture, particularly as herbicides and pesticides. Here are some intriguing points to consider:

  • Structural Diversity: The triazine ring in this compound features a unique substitution pattern, which contributes to its chemical reactivity and biological activity.
  • Chlorinated Compounds: The presence of multiple trichloromethyl groups is significant as chlorinated compounds often exhibit enhanced potency as agrochemicals due to their ability to disrupt biological processes in target organisms.
  • Selective Herbicide: This compound has been studied for its potential use as a selective herbicide, allowing for the targeting of specific weeds without harming crops.
  • Environmental Impact: As with many chlorinated compounds, interest in its bioaccumulation and environmental persistence has led to ongoing research into its degradation pathways and ecological footprint.
  • Synergistic Effects: When used in combination with other herbicides, this triazine can exhibit synergistic effects, making it more effective in controlling resistant weed populations.
  • Historical Context: Triazines have been a cornerstone in agricultural chemistry since their initial development, with ongoing efforts to improve their safety and effectiveness in modern farming practices.

As a scientist working with this compound, one might say, "Understanding the complex chemistry and environmental interactions of triazines is essential for advancing sustainable agricultural practices." Overall, this compound serves as a reminder of the intricate balance between chemical efficacy and environmental stewardship in the field of chemistry.

Synonyms
SCHEMBL1131300