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NK 0192

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Identification
Molecular formula
C19H18Cl2N2S2
CAS number
1315-09-9
IUPAC name
6-chloro-2-[5-(6-chloro-3-ethyl-1,3-benzothiazol-3-ium-2-yl)penta-2,4-dienylidene]-3-ethyl-1,3-benzothiazole
State
State

At room temperature, this compound is in a solid state, forming crystalline structures that are stable under normal conditions.

Melting point (Celsius)
255.00
Melting point (Kelvin)
528.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
529.02g/mol
Molar mass
529.0150g/mol
Density
1.3600g/cm3
Appearence

The compound appears as a dark green, crystalline powder. It is often used as a dye, indicating its vibrant color properties.

Comment on solubility

Solubility of 6-chloro-2-[5-(6-chloro-3-ethyl-1,3-benzothiazol-3-ium-2-yl)penta-2,4-dienylidene]-3-ethyl-1,3-benzothiazole

The solubility of the compound 6-chloro-2-[5-(6-chloro-3-ethyl-1,3-benzothiazol-3-ium-2-yl)penta-2,4-dienylidene]-3-ethyl-1,3-benzothiazole can be influenced by several factors, primarily its complex structure and the presence of halogen and heterocyclic groups. Here are some key points to consider:

  • Polarity: The presence of the chlorinated and benzothiazole groups suggests that this compound may exhibit moderate polarity, which could impact its interaction with polar solvents.
  • Solvent Compatibility: It is likely to be more soluble in organic solvents like dimethyl sulfoxide (DMSO), acetone, or ethanol rather than in water due to its hydrophobic characteristics.
  • Temperature Influence: The solubility may also increase with temperature, as seen with many organic compounds.
  • pH Dependence: Being a complex ionizable compound, its solubility might vary with the pH of the solution.
  • Use of Complexing Agents: The use of specific complexing agents may enhance its solubility in certain applications.

Overall, while its specific solubility parameters may require experimental confirmation, it is anticipated that this compound does have notable solubility in non-aqueous environments, making it suitable for various organic and pharmaceutical applications.

Interesting facts

Interesting Facts about 6-Chloro-2-[5-(6-chloro-3-ethyl-1,3-benzothiazol-3-ium-2-yl)penta-2,4-dienylidene]-3-ethyl-1,3-benzothiazole

This compound, often referred to by its structural components, showcases the fascinating interplay of **chlorine** and **benzothiazole** moieties. The benzothiazole group is known for its significant biological activity, often acting as a *pharmacophore* in many medicinal compounds.

Here are some notable aspects of this unique chemical entity:

  • Structure Complexity: The compound features a complex framework that includes both chlorinated and ethyl substituents, contributing to its distinct properties and potential reactions.
  • Biological Importance: Compounds with benzothiazole scaffolds are under extensive research for their roles in various biological activities, including antimicrobial and anticancer properties.
  • Applications in Organic Chemistry: This compound may serve as an intermediate in the synthesis of other valuable chemicals, especially in the development of organic materials and agrochemicals.
  • Spectroscopy Studies: The intricate bonding in this compound makes it a perfect candidate for advanced spectroscopy studies, including NMR and IR, to analyze its chemical behavior.
  • Potential for Innovation: With the ongoing studies in medicinal chemistry, this compound could inspire new drugs or treatments owing to its unique structural attributes.

As *future scientists*, understanding compounds like 6-chloro-2-[5-(6-chloro-3-ethyl-1,3-benzothiazol-3-ium-2-yl)penta-2,4-dienylidene]-3-ethyl-1,3-benzothiazole underscores the significance of *chemical diversity*. Exploring the myriad effects of halogen substitution illustrates the profound impact these elements have on reactivity and biological interactions.

In the journey of *chemical research*, one can see that the intricate world of compounds like this not only fuels our curiosity but also paves the way for *innovative discoveries* in pharmacology and material science.