1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol - 1253901-26-6
1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol
Catalog Number: BT-256979
CAS Number: 1253901-26-6
Molecular Formula: C17H17NOS
Molecular Weight: 283.389
The product is for non-human research only. Not for therapeutic or veterinary use.
Product Introduction
Description
1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol is a chemical compound that has gained significant attention in the scientific community due to its potential therapeutic and environmental applications. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, and potential applications of this compound.
Properties
CAS Number
1253901-26-6
Product Name
1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol
IUPAC Name
1-(1,3-benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol
Molecular Formula
C17H17NOS
Molecular Weight
283.389
InChI
InChI=1S/C17H17NOS/c1-11-8-9-13(12(2)10-11)17(3,19)16-18-14-6-4-5-7-15(14)20-16/h4-10,19H,1-3H3
InChI Key
IGSZVEPQZANNAB-UHFFFAOYSA-N
SMILES
CC1=CC(=C(C=C1)C(C)(C2=NC3=CC=CC=C3S2)O)C
Solubility
Soluble in DMSO
Synonyms
AC265347
Method of Synthesis or Extraction
There are several methods for synthesizing 1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol, including the reaction of 2-mercaptobenzothiazole with 2,4-dimethylbenzaldehyde in the presence of a base, or the reaction of 2-mercaptobenzothiazole with 2,4-dimethylphenacyl bromide in the presence of a base. The efficiency and yield of each method vary depending on the reaction conditions and the purity of the starting materials. Environmental and safety considerations should also be taken into account when selecting a method for synthesizing this compound.
Chemical Structure and Biological Activity
The chemical structure of 1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol consists of a benzothiazole ring and a 2,4-dimethylphenyl group attached to an ethanol molecule. This compound has been shown to exhibit potent anti-inflammatory and antioxidant activity, as well as antitumor and antimicrobial properties. The mechanism of action and biological targets of this compound are still being investigated, but it is believed to act by inhibiting various enzymes and signaling pathways involved in inflammation and oxidative stress.
Biological Effects
Studies have shown that 1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol can modulate cell function and signal transduction in various cell types, including immune cells and cancer cells. This compound has also been shown to have potential therapeutic effects in the treatment of inflammatory diseases, cancer, and microbial infections. However, it is important to note that this compound may also have potential toxic effects, and further studies are needed to determine its safety and efficacy in humans.
Applications
In medical research, 1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol has been investigated for its potential role in drug development, particularly in the treatment of inflammatory diseases and cancer. Clinical trials have shown promising results, but further studies are needed to determine its safety and efficacy in humans. In environmental research, this compound has been studied for its effects on ecosystems and its potential role in pollution management. In industrial research, it has been used in manufacturing processes to improve product quality and efficiency, but health and safety considerations should be taken into account.
Future Perspectives and Challenges
Despite the potential applications of 1-(1,3-Benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol, there are still limitations in its use and study. One of the main challenges is the lack of understanding of its mechanism of action and biological targets. Possible solutions and improvements include further studies to elucidate its mode of action and the development of more efficient and safe methods for synthesizing this compound. Future trends and prospects in the application of this compound in scientific research include the development of new drugs and therapies for inflammatory diseases and cancer, as well as its potential use in environmental and industrial applications.
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