4-Phenyl-1H-indole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a phenyl group attached to the 4-position of the indole ring, contributing to its unique chemical properties. It is typically a solid at room temperature and may exhibit a range of physical properties such as solubility in organic solvents. The presence of both aromatic and heterocyclic components in its structure allows for interesting reactivity, including potential interactions with biological systems, making it of interest in medicinal chemistry and material science. 4-Phenyl-1H-indole can participate in various chemical reactions, including electrophilic substitutions and coupling reactions, due to the electron-rich nature of the indole nitrogen. Additionally, it may exhibit fluorescence, which can be useful in various applications, including as a probe in biological studies. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

4-Phenyl-1H-indole

35577-92-5: 1H-indole, 4-phenyl-, 4-Phenylindole, 4-Phenyl-1H-indole,  4-Phenyl-1H-indole

4-phenyl-1H-indole

4-Phenyl-1H-indole is a heterocyclic organic compound that is structurally related to pyrazoles, indazoles, and other cyclic compounds. It has the chemical formula CHN and it can be found in yields of 0.2% by weight. Substituents on the 4-phenyl ring include carboxyl and cyclic structures. Reactions that can be carried out on this compound include a Diels-Alder reaction with maleic anhydride to form a heteroleptic compound. The functional group present in this molecule is the carboxylate ester.

CAS 35577-92-5: 4-Phenyl-1H-indole

4-phenyl-1H-indole

Ref: IN-DA00CKB8

4-Phenyl-1H-indole

Ref: 3D-KBA57792