2-(4-Chloro-3-nitro-phenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine

Identification

Molecular formula

C₁₃H₄Cl₇N₄O₂S

CAS number

13464-77-2

IUPAC name

2-(4-chloro-3-nitro-phenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine

State

The compound is typically in a solid state at room temperature. It is in crystalline form due to its molecular structure and interactions, which stabilize it in solid form.

Melting point (Celsius)

215.50

Melting point (Kelvin)

488.70

Boiling point (Celsius)

400.00

Boiling point (Kelvin)

673.00

General information

Molecular weight

506.40g/mol

Molar mass

506.4000g/mol

Density

1.6903g/cm³

Appearence

The compound typically appears as a yellow crystalline solid. Its crystalline form and yellow coloration are due to the presence of the nitro and chloro groups attached to the aromatic ring, contributing to its distinct appearance.

Comment on solubility

Solubility of 2-(4-chloro-3-nitro-phenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine

The solubility of 2-(4-chloro-3-nitro-phenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine can be quite intriguing due to its complex structure and the presence of various groups that influence solubility properties.

Key Factors Influencing Solubility:

Polarity: The molecule contains both polar and nonpolar groups, which can lead to a low solubility in polar solvents like water, but better solubility in nonpolar organic solvents.
Functional Groups: The presence of the trichloromethyl groups typically enhances hydrophobic interactions, further reducing solubility in water.
Hydrogen Bonding: The nitro group (-NO₂) may introduce polar character, but its influence may be outweighed by the overall hydrophobic nature of the compound.

In summary, it is likely that 2-(4-chloro-3-nitro-phenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine exhibits:

Low solubility in water: due to its nonpolar characteristics.
Higher solubility in organic solvents: such as dichloromethane or acetone.

When working with this compound, it is essential to consider these solubility properties, as they significantly impact its application and behavior in various chemical environments.

Interesting facts

Interesting Facts about 2-(4-chloro-3-nitro-phenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine

This compound, a member of the triazine family, is noteworthy for its diverse applications in various fields, including agriculture and materials science. Here are some compelling insights:

Agricultural Importance: The compound demonstrates significant herbicidal activity, making it useful in agricultural practices. Its ability to inhibit weed growth effectively contributes to higher crop yields.
Complex Structure: With its intricate framework consisting of both phenyl and triazine rings, it presents unique chemical reactivity that can be tailored for specific purposes.
Trichloromethyl Groups: The presence of trichloromethyl groups enhances its hydrophobicity and can influence its interaction with biological systems, which is an area of ongoing research.
Environmental Considerations: As with many synthetic compounds, the environmental impact is a consideration. Research is actively being conducted to assess and mitigate any potential ecological effects resulting from its use.
Synthetic Pathways: The synthesis of this compound involves several complex reactions, showcasing the fascinating chemistry involved in creating compounds with very specific functional properties.
Potential in Drug Development: The structural motifs present in triazine compounds are often explored for potential therapeutic effects, offering avenues for innovative medicinal chemistry.

In conclusion, 2-(4-chloro-3-nitro-phenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine exemplifies the intersection of functional utility and complex chemistry. As research progresses, we may uncover even more applications and insights related to this intriguing compound.

Synonyms

2-(4-chloro-3-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine

24478-15-7

DTXSID70274953