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

Identification

Molecular formula

C₉H₆Cl₆N₃

CAS number

3252-43-5

IUPAC name

2,4,6-tris(dichloromethyl)-1,3,5-triazine

State

This compound is typically found as a solid at room temperature, appearing as a crystalline substance and is not volatile under normal conditions.

Melting point (Celsius)

61.00

Melting point (Kelvin)

334.15

Boiling point (Celsius)

327.00

Boiling point (Kelvin)

600.15

General information

Molecular weight

328.89g/mol

Molar mass

328.8930g/mol

Density

1.7500g/cm³

Appearence

2,4,6-Tris(dichloromethyl)-1,3,5-triazine is a colorless compound in its pure form. Over time, or upon exposure to air, it may turn slightly yellowish. The substance usually appears as a solid crystalline powder.

Comment on solubility

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

When exploring the solubility of 2,4,6-tris(dichloromethyl)-1,3,5-triazine (C₉H₉Cl₆N₃), we encounter a compound with distinct properties. Its solubility can be influenced by a variety of factors:

Polarity: The presence of multiple dichloromethyl groups suggests that this compound may exhibit high polarity, impacting its interaction with solvents.
Solvent Compatibility: It is likely to be more soluble in organic solvents rather than in water due to its non-polar characteristics.
Temperature Dependence: Like many organic compounds, its solubility can also increase with temperature, which can enhance molecular movement and solvation.

A valuable point to remember is that compounds with multiple chlorine substituents can often struggle with solubility in aqueous environments. This results in limited use in certain applications where water solubility is crucial.

Conclusively, the solubility of 2,4,6-tris(dichloromethyl)-1,3,5-triazine is subject to its molecular structure, symmetry, and environmental conditions, establishing it as an intriguing subject for further studies.

Interesting facts

Interesting Facts about 2,4,6-Tris(dichloromethyl)-1,3,5-triazine

2,4,6-Tris(dichloromethyl)-1,3,5-triazine, often abbreviated as TDT, is a fascinating compound that showcases the intricate world of heterocyclic chemistry. Here are some engaging insights about this compound:

Structural Beauty: TDT features a triazine ring, which consists of three nitrogen atoms and three carbon atoms arranged in a six-membered ring. The presence of dichloromethyl groups enhances its chemical reactivity and opens up various avenues for synthetic applications.
Versatile Applications: TDT has gained attention in the field of agrochemicals for its potential use as a herbicide. Its ability to interact with specific biological pathways makes it a compound of interest in developing targeted treatments for pests.
Unique Reactivity: The dichloromethyl groups contribute to the compound's electrophilic nature, allowing it to participate in various nucleophilic substitution reactions. This characteristic can be exploited to synthesize more complex organic molecules.
Research Potential: TDT has been the subject of numerous studies exploring its properties and functionalities. According to one researcher, "TDT serves as a valuable scaffold for the design of novel compounds in both medicinal and agricultural chemistry."
Environmental Considerations: While TDT demonstrates remarkable effectiveness in its applications, scientists are also investigating its environmental impact. Understanding its degradation pathways and mitigating its potential toxicity are crucial areas of ongoing research.

In conclusion, 2,4,6-Tris(dichloromethyl)-1,3,5-triazine stands as a prime example of how a seemingly simple compound can lead to complex chemistry and innovative applications, capturing the attention of both chemists and environmental scientists alike.

Synonyms

5311-21-7

s-Triazine, 2,4,6-tris(dichloromethyl)-

2,4,6-TRIS(DICHLOROMETHYL)-S-TRIAZINE

SCHEMBL81344

DTXSID70201204