CAS 26340-49-8
:1H-Indole, 2-iodo-
Description:
1H-Indole, 2-iodo- is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of an iodine atom at the second position 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 aromatic characteristics, contributing to its stability and potential applications in various chemical reactions. It is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in electrophilic substitution reactions. Additionally, 1H-Indole, 2-iodo- can serve as a precursor for the synthesis of more complex molecules. Its iodine substituent can also facilitate further functionalization, making it a valuable intermediate in synthetic chemistry. Safety precautions should be observed when handling this compound, as iodine can be hazardous, and appropriate storage conditions should be maintained to ensure stability.
Formula:C8H6IN
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Found 5 products.
2-Iodo-1H-indole
CAS:2-Iodo-1H-indoleFormula:C8H6INPurity:95%Color and Shape: brown solidMolecular weight:243.04g/mol2-Iodoindole
CAS:<p>2-Iodoindole is a chemical compound that is a member of the amide family. The 2-iodoindole skeleton is found in many biologically active compounds, including anti-viral agents, such as acyclovir and ribavirin. The acylation reaction of 2-iodoindole with an acid chloride yields a racemic mixture of enantiomers, which can be separated by recrystallization from water. 2-Iodoindole also reacts with sodium to form the salt sodium 2-iodoindolate, which has been shown to inhibit plant root formation.<br>2-Iodoindoles are not known to be efficient for the synthesis of other chemical compounds due to their low reaction yield and high reactivity with water.</p>Formula:C8H6INPurity:Min. 95%Molecular weight:243.04 g/mol
