CAS 54466-88-5
:(1H-indol-3-ylsulfanyl)acetate
Description:
(1H-indol-3-ylsulfanyl)acetate, with the CAS number 54466-88-5, is a chemical compound that features an indole ring structure substituted with a sulfanyl (thioether) group and an acetate moiety. This compound is characterized by its unique combination of an indole, which is known for its aromatic properties and biological significance, particularly in pharmaceuticals and natural products. The presence of the sulfanyl group introduces potential for reactivity and interaction with various biological systems, making it of interest in medicinal chemistry. The acetate group contributes to the compound's solubility and stability, influencing its behavior in biological and chemical environments. Overall, (1H-indol-3-ylsulfanyl)acetate exhibits properties typical of indole derivatives, including potential antioxidant and anti-inflammatory activities, and may serve as a scaffold for further chemical modifications in drug development. Its specific applications and reactivity would depend on the context of its use in research or industry.
Formula:C10H9NO2S
InChI:InChI=1/C10H9NO2S/c12-10(13)6-14-9-5-11-8-4-2-1-3-7(8)9/h1-5,11H,6H2,(H,12,13)/p-1
SMILES:c1ccc2c(c1)c(c[nH]2)SCC(=O)[O-]
Synonyms:- 2-((1H-indol-3-yl)thio)acetic acid
- (1H-INDOL-3-YLSULFANYL)-ACETIC ACID
- (1H-Indol-3-ylsulfonyl)acetic acid
- Acetic acid, 2-(1H-indol-3-ylthio)-
- (1{H}-indol-3-ylthio)acetic acid
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Found 2 products.
(1H-Indol-3-ylsulfanyl)-acetic acid
CAS:<p>(1H-Indol-3-ylsulfanyl)-acetic acid is a versatile compound with various applications. It serves as an active agent in the synthesis of several important compounds, including cellulose derivatives, lapatinib, pyrazoles, and sulfonyl compounds. This compound is widely used in industrial settings as a synthetic intermediate for the production of various chemicals.</p>Formula:C10H9NO2SPurity:Min. 95%Molecular weight:207.25 g/mol
