Interesting facts
Interesting Facts about 2-(1,3-benzothiazol-2-ylsulfanyl)ethanol
2-(1,3-benzothiazol-2-ylsulfanyl)ethanol is a fascinating compound with various intriguing properties and applications in the field of chemistry. Here are some highlights:
- Structural Significance: This compound contains a unique benzothiazole moiety, which is known for its diverse electronic properties and biological activities. The sulfenyl group adds a layer of reactivity that can be harnessed in synthesis.
- Biological Relevance: Compounds containing benzothiazole derivatives have been studied for their potential anti-cancer, anti-inflammatory, and antimicrobial activities. Some researchers are intrigued by how the specific structure of this compound might influence its biological effectiveness.
- Synthetic Utility: The presence of both hydroxyl and thioether functional groups makes 2-(1,3-benzothiazol-2-ylsulfanyl)ethanol a valuable intermediate in organic synthesis. It can serve as a precursor for more complex molecules in pharmaceutical chemistry.
- Analytical Interest: The unique absorbance properties of the benzothiazole component make this compound useful in the design of chemosensors and probes for detecting metal ions, which are essential in environmental monitoring.
- Multifaceted Applications: With its array of functional groups, this compound could find applications not only in medicinal chemistry but also in materials science, possibly contributing to the development of new polymers or coatings.
As a student of chemistry, exploring the unique characteristics of 2-(1,3-benzothiazol-2-ylsulfanyl)ethanol can illuminate the pathways through which compounds with specialized structures contribute to the advancement of science and technology.
Synonyms
2-(2-Benzothiazolylthio)ethanol
4665-63-8
2-(2-Hydroxyethylmercapto)benzothiazole
BENZOTHIAZOLE, 2-(2-HYDROXYETHYLTHIO)-
DTXSID00196896
DTXCID40119387
625-976-0
2-(1,3-Benzothiazol-2-ylsulfanyl)ethanol
2-(1,3-benzothiazol-2-ylsulfanyl)ethan-1-ol
2-(Benzo[d]thiazol-2-ylthio)ethanol
HMBT
Ethanol, 2-(2-benzothiazolylthio)-
Maybridge3_005653
Cambridge id 5108936
CBDivE_013692
SCHEMBL745752
HMS1447A21
AKOS000635128
2-(Benzothiazol-2-ylsulfanyl)-ethanol
2-(2-Benzothiazolylthio)ethanol, 95%
IDI1_017040
2-(2-hydroxyethylmercapto) benzothiazole
2-(Benzo[d]thiazol-2-ylthio)ethan-1-ol
AS-60773
CS-0358808
NS00007054
2-(1,3-Benzothiazol-2-ylsulfanyl)ethanol #
AB00073871-01
InChI=1/C9H9NOS2/c11-5-6-12-9-10-7-3-1-2-4-8(7)13-9/h1-4,11H,5-6H
Solubility of 2-(1,3-benzothiazol-2-ylsulfanyl)ethanol
2-(1,3-benzothiazol-2-ylsulfanyl)ethanol is a compound that exhibits unique solubility characteristics. Understanding its solubility is crucial for various applications, including pharmacology and material science. Here are some key points regarding its solubility:
In summary, while 2-(1,3-benzothiazol-2-ylsulfanyl)ethanol displays favorable solubility in polar solvents, its overall solubility profile is influenced by various factors such as temperature, pH, and the presence of other solutes. This makes it a versatile compound for researchers in the field.