CAS 57817-08-0
:1H-Indole, 6,7-dichloro-
Description:
1H-Indole, 6,7-dichloro- is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of two chlorine atoms at the 6 and 7 positions of the indole ring significantly influences its chemical properties and reactivity. This compound is typically a solid at room temperature and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. It may exhibit properties such as antimicrobial, antifungal, or anticancer activities, making it of interest in medicinal chemistry. The dichlorination introduces electron-withdrawing effects, which can alter the compound's reactivity and interaction with biological targets. Additionally, 1H-Indole, 6,7-dichloro- is likely to be soluble in organic solvents, while its solubility in water may be limited. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks. Overall, this compound represents a significant area of study in organic and medicinal chemistry.
Formula:C8H5Cl2N
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Found 4 products.
1H-Indole, 6,7-dichloro-
CAS:Formula:C8H5Cl2NPurity:98%Color and Shape:SolidMolecular weight:186.03806,7-Dichloro-1H-indole
CAS:<p>6,7-Dichloro-1H-indole is a non-steroidal compound that has shown to have pharmacological activity in vivo. It is an acidic compound with a pKa of 4.5 and can be found in venoms such as those of the snake genus Echis and other snakes. 6,7-Dichloro-1H-indole has been shown to inhibit the enzymatic activity of hyaluronidases and acid moieties, which are found in Streptococcus pyogenes and other streptococci. This compound also inhibits the production of toxins from these bacteria and has been shown to damage extracellular matrix proteins in vivo.</p>Formula:C8H5NCl2Purity:Min. 95%Molecular weight:186.03 g/mol
