2,4-dimethyl-6-(methylthio)-1,3,5-triazine

Identification

Molecular formula

C₆H₉N₃S

CAS number

25259-39-2

IUPAC name

2,4-dimethyl-6-methylsulfanyl-1,3,5-triazine

State

At room temperature, 2,4-dimethyl-6-(methylthio)-1,3,5-triazine is generally found in a solid state. It maintains stability under standard conditions, maintaining its crystalline form.

Melting point (Celsius)

62.00

Melting point (Kelvin)

335.15

Boiling point (Celsius)

253.00

Boiling point (Kelvin)

526.15

General information

Molecular weight

155.22g/mol

Molar mass

155.2210g/mol

Density

1.1800g/cm³

Appearence

2,4-Dimethyl-6-(methylthio)-1,3,5-triazine typically appears as a white crystalline powder. Its purity and specific grain size can influence its exact appearance, which is often characterized by a fine, uniform texture typical for crystalline compounds.

Comment on solubility

Solubility of 2,4-Dimethyl-6-methylsulfanyl-1,3,5-triazine

The compound 2,4-dimethyl-6-methylsulfanyl-1,3,5-triazine presents a unique profile when discussing its solubility. Understanding solubility is critical, as it governs the compound's effectiveness in various applications, particularly in biological and environmental contexts.

Here are some key considerations regarding its solubility:

Polarity: The presence of methyl groups and the methylsulfanyl functional group contributes to the overall polarity of the molecule, which can affect its solubility in different solvents.
Solvent Compatibility: Generally, compounds with higher polarity tend to be more soluble in polar solvents (like water), while non-polar compounds dissolve better in non-polar solvents (like hexane). The solubility of this triazine compound in various solvents can vary significantly.
Hydrogen Bonding: If the compound can form hydrogen bonds, it may enhance its solubility in polar solvents. However, the degree to which this compound can participate in hydrogen bonding is limited due to its structure.
Concentration Effects: At higher concentrations, solubility can decrease due to interactions between solute molecules, leading to saturation.

As a general trend, many triazine derivatives exhibit poor water solubility, which may also be the case for 2,4-dimethyl-6-methylsulfanyl-1,3,5-triazine. This characteristic may limit its use in aqueous environments but potentially enhances its application in organic solvents.

In summary, while solubility profiles can vary widely, the interaction of functional groups within 2,4-dimethyl-6-methylsulfanyl-1,3,5-triazine with potential solvents is an essential aspect of its usage and effectiveness. Understanding these nuances is crucial for chemists and researchers working with this compound.

Interesting facts

Interesting Facts about 2,4-Dimethyl-6-methylsulfanyl-1,3,5-triazine

2,4-Dimethyl-6-methylsulfanyl-1,3,5-triazine is a fascinating compound that belongs to the triazine family, characterized by its unique three-ring structure containing nitrogen atoms. This compound has gained attention in various fields of scientific research due to its potential applications and intriguing chemical properties.

Key Features and Applications

Agricultural Relevance: Compounds like this triazine derivative can serve as effective herbicides. Their selective action allows for the control of pest species while minimizing damage to crops.
Pharmaceutical Potential: Research into similar triazine structures has led to the discovery of compounds with anti-cancer properties. This raises excitement about the potential medicinal applications of 2,4-dimethyl-6-methylsulfanyl-1,3,5-triazine.
Versatile Synthesis: The synthesis of this compound can be achieved through various methods, making it an accessible target for organic chemists. Its reactivity provides opportunities for creating other structurally related molecules.
Research in Material Science: The triazine ring system can contribute to the development of polymers and novel materials, leading to innovations in material science.

Noteworthy Characteristics

This compound is noted for its substituent pattern, which influences its reactivity and biological interactions. The presence of both methyl and methylsulfanyl groups highlights the versatility of triazine derivatives in modulating chemical properties.

Moreover, 2,4-dimethyl-6-methylsulfanyl-1,3,5-triazine serves as a great teaching tool for students delving into organic chemistry. It exemplifies how structural variations can affect chemical behavior and applications, making it a valuable subject in both academic and research contexts.

In conclusion, the study of 2,4-dimethyl-6-methylsulfanyl-1,3,5-triazine exemplifies the rich interplay between structure and functionality in organic compounds. As researchers continue to explore its potential, who knows what new and exciting applications may arise!

Synonyms

SCHEMBL19000175