4,6-bis(allylamino)-1,3,5-triazine-2-thiol

Identification

Molecular formula

C₉H₁₁N₅S

CAS number

17520-49-3

IUPAC name

4,6-bis(allylamino)-1,3,5-triazine-2-thiol

State

At room temperature, this compound is typically found in a solid state, often as a crystalline substance.

Melting point (Celsius)

172.00

Melting point (Kelvin)

445.15

Boiling point (Celsius)

324.00

Boiling point (Kelvin)

597.15

General information

Molecular weight

236.28g/mol

Molar mass

236.3000g/mol

Density

1.3210g/cm³

Appearence

The compound typically presents as a powder or crystalline solid. Its color may vary slightly based on the purity and specific formulation, but it is commonly off-white or light-colored.

Comment on solubility

Solubility of 4,6-bis(allylamino)-1,3,5-triazine-2-thiol

The compound 4,6-bis(allylamino)-1,3,5-triazine-2-thiol exhibits intriguing solubility characteristics due to its unique molecular structure. Solubility can greatly influence its application in various fields such as pharmaceuticals and agriculture. Here are some key points regarding its solubility:

Polar vs. Nonpolar: The presence of both amino groups and a thiol functional group may enhance its polarity, making it more soluble in polar solvents, such as water.
Organic Solvents: This compound could also be compatible with a range of organic solvents, particularly those that can dissolve other nitrogenous or sulfur-containing compounds.
pH Dependence: The solubility may be further influenced by the pH of the solution, as protonation of the amino groups could alter its solubility profile.
Temperature Influence: Like many compounds, solubility may increase with temperature, suggesting that heating solutions could enhance the dissolution of 4,6-bis(allylamino)-1,3,5-triazine-2-thiol.

In summary, while the exact solubility parameters may need to be empirically determined for specific conditions, understanding these factors can provide valuable insights into the potential applications of 4,6-bis(allylamino)-1,3,5-triazine-2-thiol.

Interesting facts

Interesting Facts about 4,6-bis(allylamino)-1,3,5-triazine-2-thiol

4,6-bis(allylamino)-1,3,5-triazine-2-thiol is a fascinating compound that belongs to the class of triazines, which are known for their diverse range of applications in both industrial and medicinal fields. Here are some intriguing facts about this compound:

Versatile Applications: This compound is commonly recognized for its utility in the fields of agriculture and pharmaceuticals, particularly as an effective herbicide and in the development of certain medicaments.
Synthesized through Unique Pathways: The synthesis of this compound often involves unique chemical reactions that showcase the creativity and ingenuity required in organic chemistry.
Importance of Thiol Group: The presence of the thiol (-SH) group in its structure is noteworthy, as thiols are known for their reactivity and their role in various biological systems, especially in forming disulfide bonds and their involvement in enzymatic functions.
Stability and Reactivity: The dual functionality of the allylamino groups provides interesting dynamics in terms of stability and reactivity, allowing chemists to explore various derivatives and modifications.
Polymerization Potential: Due to its structure, this compound has the potential to participate in polymerization reactions, paving the way for creating new materials with unique properties.

In summary, 4,6-bis(allylamino)-1,3,5-triazine-2-thiol not only showcases the vast and complex nature of organic chemistry but also emphasizes the importance of studying such compounds to unlock their true potential in various applications across multiple fields. The unique characteristics and functionalities this compound offers make it a subject of interest for ongoing research and innovation.