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

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Identification
Molecular formula
C6H6Cl2N3S
CAS number
69490-21-1
IUPAC name
2-allylsulfanyl-4,6-dichloro-1,3,5-triazine
State
State

At room temperature, 2-allylthio-4,6-dichloro-1,3,5-triazine is typically found in a solid state, characterized by its crystalline structure.

Melting point (Celsius)
70.00
Melting point (Kelvin)
343.15
Boiling point (Celsius)
333.00
Boiling point (Kelvin)
606.15
General information
Molecular weight
224.10g/mol
Molar mass
224.0800g/mol
Density
1.4700g/cm3
Appearence

The compound appears as a crystalline solid that can range from off-white to light yellow in color, depending on purity and storage conditions.

Comment on solubility

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

When examining the solubility of 2-allylsulfanyl-4,6-dichloro-1,3,5-triazine, we can consider various factors that influence how this compound interacts with solvents. Here are some key points to keep in mind:

  • Polarity: The presence of both allyl and chloro groups affects the overall polarity of the molecule, which can significantly influence its solubility in polar versus nonpolar solvents.
  • Hydrogen Bonding: Given the structural components, hydrogen bonding capabilities may also play a role in how well the compound dissolves in various mediums.
  • Solvent Compatibility: This compound may show improved solubility in organic solvents such as ethanol or dimethyl sulfoxide (DMSO), while exhibiting limited solubility in polar protic solvents like water.
  • Environmental Factors: Temperature and concentration can further impact solubility; generally, higher temperatures increase solubility.

Understanding the solubility of 2-allylsulfanyl-4,6-dichloro-1,3,5-triazine is crucial for applications in synthetic chemistry and formulation processes. As such, conducting solubility tests across different solvents is essential to determine the most suitable conditions for its use.

Interesting facts

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

2-allylsulfanyl-4,6-dichloro-1,3,5-triazine is an intriguing compound that highlights the versatility of triazine derivatives in chemistry. Here are some fascinating points about this compound:

  • Triazine Framework: The triazine ring structure, characterized by three nitrogen atoms in a six-membered ring, provides unique chemical reactivity that is extensively exploited in agricultural and pharmaceutical chemistry.
  • Biological Activity: Compounds featuring a triazine core often exhibit significant biological activities, including herbicidal and fungicidal properties. This makes them valuable in the development of agrochemicals.
  • Diverse Substitution: The presence of various functional groups, such as the allylsulfanyl and dichloro regions, allows for a wide range of chemical transformations, rendering the compound applicable in synthetic organic chemistry.
  • Research and Development: Ongoing studies examine the synthesis and application of triazines like this one, aiming to enhance their efficacy and reduce environmental impact in agricultural practices.
  • Structural Variability: Changing the substituents on the triazine ring can lead to different properties and functionalities, making this a rich area for research in material science and drug discovery.

As a reminder, the realm of triazine chemistry continues to evolve, showcasing the importance of studying derivatives like 2-allylsulfanyl-4,6-dichloro-1,3,5-triazine to unlock new potentials in various fields.

Synonyms
25713-56-8
2-(Allylthio)-4,6-dichloro-1,3,5-triazine
SCHEMBL9723466