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

Identification

Molecular formula

C₈H₁₄N₆S

CAS number

53980-62-8

IUPAC name

2-(diazonioamino)-4-(isopropylamino)-6-methylsulfanyl-1,3,5-triazine

State

At room temperature, this compound exists as a solid. It is not typically volatile under standard conditions, which makes it easier to handle and store. The solid state is preferred for many of its applications due to the stability it offers.

Melting point (Celsius)

175.00

Melting point (Kelvin)

448.00

Boiling point (Celsius)

255.00

Boiling point (Kelvin)

528.00

General information

Molecular weight

230.29g/mol

Molar mass

230.2910g/mol

Density

1.3600g/cm³

Appearence

This compound typically appears as a crystalline solid. It has a distinct appearance due to its unique structure, and it is often colorless or light-colored. As a stable triazine derivative, it exhibits characteristics typical of such compounds, forming regular crystalline shapes under controlled conditions.

Comment on solubility

Solubility of 2-(diazonioamino)-4-(isopropylamino)-6-methylsulfanyl-1,3,5-triazine

The solubility of 2-(diazonioamino)-4-(isopropylamino)-6-methylsulfanyl-1,3,5-triazine, often referred to as a complex organic compound, is influenced by various factors. Understanding its solubility can significantly impact its practical applications in chemical reactions and formulations. Here are some key considerations:

Polarity: As a molecule with both polar (amino) and nonpolar (isopropyl) regions, its solubility can vary depending on the solvent used.
Solvent Choice: Generally, this compound would be more soluble in polar solvents such as water or alcohols.
Effect of Temperature: Increased temperature often enhances solubility for organic compounds, providing greater interaction between solute and solvent.
Concentration of Solvents: The presence of other solutes can significantly affect solubility, either promoting or creating a barrier to dissolution.

In summary, the solubility of 2-(diazonioamino)-4-(isopropylamino)-6-methylsulfanyl-1,3,5-triazine is not absolute and can vary widely based on the aforementioned factors, making it essential to carry out specific experiments to ascertain its solubility in desired conditions.

Interesting facts

Interesting Facts about 2-(diazonioamino)-4-(isopropylamino)-6-methylsulfanyl-1,3,5-triazine

The compound 2-(diazonioamino)-4-(isopropylamino)-6-methylsulfanyl-1,3,5-triazine is a fascinating example of a substituted triazine, showcasing the intricate world of organic synthesis and compound modification. Here are some engaging facts about this particular compound:

Structure and Functionality: The unique arrangement of nitrogen and sulfur atoms in the triazine ring contributes to its chemical reactivity, offering potential applications in pharmaceutical and agricultural chemistry.
Versatile Applications: Compounds like this are crucial in the development of herbicides, pesticides, and pharmaceuticals. The triazine backbone is often a key component in agrochemical formulations due to its ability to inhibit certain biological pathways in target organisms.
Diverse Molecular Modifications: The existence of functional groups such as diazonium, isopropylamino, and methyl sulfanyl allows for various derivatizations, enhancing the compound's properties and applications.
Innovative Synthetic Pathways: The synthesis of this compound involves intricate multi-step reactions, highlighting the ingenuity involved in organic chemistry. This compound can serve as a model for studying reaction mechanisms and kinetics.
Color Change as an Indicator: Certain derivatives of diazonium compounds are known for their ability to impart color changes in solutions, making them useful as dyes or indicators in various chemical analyses.

As you delve deeper into the world of triazines and their derivatives, remember that every compound tells a story of discovery, reaction pathways, and potential. This particular compound exemplifies the creativity and complexity inherent in the field of organic chemistry.