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

Identification

Molecular formula

C₇H₁₀Cl₂N₃S

CAS number

24279-39-8

IUPAC name

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

State

At room temperature, 2,4-dichloro-6-isobutylsulfanyl-1,3,5-triazine is typically found as a solid. Its crystalline form makes it a stable compound under standard conditions.

Melting point (Celsius)

75.00

Melting point (Kelvin)

348.15

Boiling point (Celsius)

353.00

Boiling point (Kelvin)

626.15

General information

Molecular weight

266.17g/mol

Molar mass

266.1680g/mol

Density

1.4800g/cm³

Appearence

2,4-Dichloro-6-isobutylsulfanyl-1,3,5-triazine typically appears as a solid crystalline powder. It is characterized by its dichloro substituents and the presence of an isobutylsulfanyl group, which can influence its solubility and reactivity.

Comment on solubility

Solubility of 2,4-Dichloro-6-isobutylsulfanyl-1,3,5-triazine

When considering the solubility of 2,4-dichloro-6-isobutylsulfanyl-1,3,5-triazine, several key factors come into play:

Polarity of the Compound: The presence of chlorine (Cl) and sulfur (S) atoms in the molecular structure contributes to the overall polarity. Chlorine, being highly electronegative, can enhance the compound's interaction with polar solvents.
Hydrophobic and Hydrophilic Regions: The isobutyl group adds a hydrophobic characteristic, which may limit solubility in water but enhance solubility in organic solvents.
Common Solvents: This compound tends to be more soluble in non-polar and weakly polar solvents, such as ethanol or dimethyl sulfoxide (DMSO), rather than in water.

In summary, the solubility of 2,4-dichloro-6-isobutylsulfanyl-1,3,5-triazine is influenced by its structural features and the nature of the solvent. As a rule of thumb, *like dissolves like*: non-polar compounds will be more soluble in non-polar solvents, while polar compounds are favored in polar solvents.

Interesting facts

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

2,4-dichloro-6-isobutylsulfanyl-1,3,5-triazine, commonly referred to in the field of chemistry as a substituted triazine compound, exhibits fascinating characteristics and applications:

Phytotoxic Effects: This compound has demonstrated significant phytotoxic activity, making it a subject of interest in agricultural research. Its ability to inhibit the growth of certain plants allows for its potential use as a selective herbicide.
Synthesis Pathways: The synthesis of triazine compounds typically involves reaction mechanisms such as cyclization or nucleophilic substitution, making 2,4-dichloro-6-isobutylsulfanyl-1,3,5-triazine an intriguing example of synthetic organic chemistry.
Importance in the Synthesis of Other Compounds: Compounds with a triazine core, like this one, serve as valuable intermediates in the production of a variety of agrochemical products and pharmaceuticals, showcasing their versatility.
Environmental Impact: As studies continue, understanding the environmental behavior of this compound is crucial. Its effects on non-target organisms and its breakdown products can provide insights on ecological safety.
Research Potential: Ongoing research aims to explore modifications of this compound to enhance its herbicidal properties while minimizing environmental impact. Scientists are particularly interested in structural variations that can lead to more effective and environmentally benign alternatives.

In summary, 2,4-dichloro-6-isobutylsulfanyl-1,3,5-triazine stands out as a compound rich in potential applications, particularly within agrochemistry, and offers an exciting landscape for further scientific inquiry.

Synonyms

AKOS012164565