Cyanuric chloride
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- Molecular formula
- C3N3Cl3
- CAS Number
- 108-77-0
- IUPAC Name
- 2,4-dichloro-1,3,5-triazine
- Molecular Weight
- 145.00g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3203g/cm3
- Synonyms
- 2, 4-Dichloro-1, 3, 5-triazine
Identification
Interesting facts
Fascinating Insights into 2,4-Dichloro-1,3,5-triazine
2,4-Dichloro-1,3,5-triazine is a notable compound in the field of chemistry, particularly due to its applications and unique structural characteristics. Here are some interesting facts:
- Structure and Stability: This compound features a triazine ring structure, which is a six-membered aromatic ring containing three nitrogen atoms. This cyclic structure contributes to its stability and reactivity.
- Herbicide Applications: 2,4-Dichloro-1,3,5-triazine is largely used in the agricultural sector as a herbicide, particularly for controlling weeds in various crops. It is known for its selective action, allowing it to target unwanted flora without harming the crops.
- Synthesis Pathways: There are several synthetic routes to produce this compound, one of which involves chlorination of cyanuric chloride. Understanding these pathways is essential for chemists to enhance yield and efficiency.
- Importance of Functional Groups: The presence of chlorine atoms in the 2 and 4 positions significantly affects the compound's reactivity and biological activity, making it a subject of interest for further chemical modifications and studies.
- Environmental Considerations: The use of chlorinated compounds in agriculture raises questions regarding environmental persistence and toxicity. Scientists are actively researching ways to mitigate any adverse effects associated with its use.
As a chemistry student or researcher, studying 2,4-dichloro-1,3,5-triazine provides insights into different fields such as organic synthesis, environmental science, and agricultural chemistry. The dual challenges of maximizing its functionality while minimizing ecological impact make it an intriguing topic for future investigation.