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6-Aminobenzothiazole-2-thiol

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Identification
Molecular formula
C7H6N2S2
CAS number
16409-45-3
IUPAC name
6-amino-1,3-benzothiazole-2-thiol
State
State

At room temperature, 6-Aminobenzothiazole-2-thiol is in a solid state.

Melting point (Celsius)
218.00
Melting point (Kelvin)
491.15
Boiling point (Celsius)
468.00
Boiling point (Kelvin)
741.15
General information
Molecular weight
168.26g/mol
Molar mass
168.2600g/mol
Density
1.5160g/cm3
Appearence

6-Aminobenzothiazole-2-thiol appears as a yellow to orange crystalline solid. It is usually free-flowing and its color can vary slightly depending on purity and specific formulation.

Comment on solubility

Solubility of 6-amino-1,3-benzothiazole-2-thiol

6-amino-1,3-benzothiazole-2-thiol, with its unique structure, exhibits interesting solubility characteristics in various solvents. This compound is generally considered to be soluble in polar solvents, which can significantly influence its potential applications in different chemical processes.

Key factors affecting the solubility of 6-amino-1,3-benzothiazole-2-thiol include:

  • Polarity: The presence of amino and thiol functional groups enhances its interaction with polar solvents like water and alcohols.
  • Hydrogen bonding: The ability to form hydrogen bonds due to the -NH2 and -SH groups improves its solubility profile.
  • Temperature: Higher temperatures may increase solubility, as is common with many organic compounds.

In practice, it is often found that:

  • It is sparingly soluble in non-polar solvents such as hexane or toluene.
  • When dissolved, the compound can exist in multiple tautomeric forms, further influencing its solubility dynamics.

Ultimately, understanding the solubility of 6-amino-1,3-benzothiazole-2-thiol is crucial for its use in various chemical applications, enabling effective formulation in reactions and processes.

Interesting facts

Interesting Facts about 6-Amino-1,3-benzothiazole-2-thiol

6-Amino-1,3-benzothiazole-2-thiol is a fascinating compound with a variety of applications in both chemical research and industry. Here are some noteworthy aspects of this compound:

  • Structural Significance: The compound features a benzothiazole ring, which is known for its stability and versatility in various chemical reactions. This structure contributes to its unique chemical properties.
  • Biological Relevance: Compounds of this category have been studied for their potential biological activities, including antimicrobial and antitumor effects. Researchers are continually exploring how such compounds can be leveraged in medicinal chemistry.
  • Analytical Applications: 6-Amino-1,3-benzothiazole-2-thiol is often used in analytical chemistry for the detection of metal ions. Its ability to form complexes with metals makes it valuable for environmental monitoring and quality control in various industries.
  • Versatile Reactions: This thiol compound can participate in various chemical reactions, such as nucleophilic substitution and redox reactions, making it a versatile building block for synthesizing more complex organic molecules.
  • Safety Precautions: While studying this compound, it is essential to consider proper laboratory practices. As with many sulfur-containing compounds, precautions should be taken to handle it safely due to the potential for toxicity.

In summary, 6-amino-1,3-benzothiazole-2-thiol is not just a simple organic compound; it embodies a range of functionalities that spark the interest of both chemists and biologists. The continuing research in this area aims to uncover even more possibilities and applications for this intriguing molecule.