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2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine

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Identification
Molecular formula
C10H6Cl2N3S
CAS number
21524-48-1
IUPAC name
2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine
State
State

At room temperature, 2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine is found in a solid state. Its state of aggregation as a solid makes it easy to weigh and handle for chemical synthesis or reactive processes.

Melting point (Celsius)
72.00
Melting point (Kelvin)
345.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
297.14g/mol
Molar mass
297.1400g/mol
Density
1.4567g/cm3
Appearence

2-Benzylsulfanyl-4,6-dichloro-1,3,5-triazine appears as a solid compound, typically in a crystalline or powder form. The substance may have a light yellow to off-white coloration, depending on its purity and preparation method.

Comment on solubility

Solubility of 2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine

The solubility of 2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine is a critical factor that defines its application and behavior in various environments. This compound, due to its structural complexity, exhibits certain solubility characteristics:

  • Polar Characteristics: The presence of chloro groups typically enhances interaction with polar solvents, though theTriazine ring itself can display limited solubility in water.
  • Organic Solvents: It is generally more soluble in organic solvents like ethanol, acetone, or dimethyl sulfoxide (DMSO), making it amenable for use in organic synthesis and formulations.
  • Temperature Dependency: Solubility can vary significantly with temperature; typically, increasing temperature may enhance solubility in organic solvents.

As with many organic compounds, the structure-solubility relationship plays a pivotal role; thus, the presence of functional groups like the benzylsulfanyl moiety can both promote and hinder solubility depending on the solvent used. In conclusion, understanding the solubility profile of 2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine is essential for its effective utilization in various chemical processes.

Interesting facts

Interesting Facts about 2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine

2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine is a fascinating compound that falls within the broad category of triazine derivatives. Its unique structure and functionalities give rise to several intriguing characteristics and applications, making it a notable topic of study in the field of chemistry.

Unique Characteristics

  • Triazine Framework: The triazine ring system is known for its stability and versatility. This compound features a five-membered aromatic ring containing nitrogen atoms, which enhances its chemical reactivity.
  • Sulfur Presence: The benzylsulfanyl group introduces a sulfur atom to the molecule, which can impart distinct chemical properties, including enhanced nucleophilicity.
  • Chloro Substituents: With two chlorine atoms positioned on the ring, this compound may exhibit increased reactivity in electrophilic aromatic substitution reactions, making it an attractive target in further synthetic transformations.

Potential Applications

The unique composition of this compound renders it useful in various fields:

  • Agricultural Chemistry: Compounds like this one can act as herbicides or fungicides owing to their ability to disrupt biological pathways in target organisms.
  • Pharmaceutical Research: The dichloro-triazine framework and sulfanyl group may influence biological activity, offering potential for developing new therapeutic agents.
  • Material Science: Its properties can be leveraged in creating new materials with desirable characteristics such as resistance to degradation or enhanced thermal stability.

Challenges in Study

Despite its intriguing properties, studying 2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine poses some challenges:

  • Synthetic Complexity: The synthesis of this compound may require advanced organic methodologies, making it less accessible for routine laboratory work.
  • Reactivity Management: The presence of reactive functional groups necessitates careful handling and consideration of safety protocols during experimentation.

In summary, 2-benzylsulfanyl-4,6-dichloro-1,3,5-triazine exemplifies the rich diversity of chemical compounds, offering avenues for research across various scientific domains. Its unique structure not only contributes to its reactive potential but also underscores the importance of continued exploration in the realm of triazine chemistry.

Synonyms
25713-57-9
DTXSID90275023
2-(benzylsulfanyl)-4,6-dichloro-1,3,5-triazine
RefChem:253274
DTXCID10226471
2-(Benzylthio)-4,6-dichloro-1,3,5-triazine
SCHEMBL5888974
AKOS009154377