3-Phenylindole

3-Phenylindole (CAS 1504-16-1) is a classic aromatic indole heterocyclic compound with a phenyl group attached to the 3-position of the indole ring. This compound has excellent photoelectric performance, good thermal stability and strong fluorescence characteristics. It features a conjugated π-electron system formed by indole ring and benzene ring, showing outstanding light absorption and luminescence properties. The active NH group on indole ring supports electrophilic substitution, coupling and alkylation reactions. As a mainstream functional indole building block, 3-Phenylindole (CAS 1504-16-1) is widely used in organic photoelectric materials, pharmaceutical synthesis, fluorescent probes and fine organic synthesis fields.

3-Phenyl-1H-indole, 1H-Indole, 3-phenyl-, NSC 76690, 3-Phenylindol

2933990099

1. Organic Optoelectronic Material Intermediate: 3-Phenylindole (CAS 1504-16-1) is a core raw material for preparing OLED hole transport materials, luminescent layer materials and organic photodetector materials. Its stable conjugated structure can improve device thermal stability and luminous efficiency, and reduce the driving voltage of optoelectronic devices, which is commonly used in laboratory organic semiconductor material research. 2. Pharmaceutical Synthetic Intermediate: This phenyl-substituted indole derivative is applied to synthesize anti-cancer drugs, anti-inflammatory agents and central nervous system regulatory drugs. The rigid aromatic conjugated structure can enhance the binding ability of drug molecules to biological targets, improve metabolic stability and bioavailability, and accelerate the screening of indole-based new drug candidates. 3. Fluorescent Probe Raw Material: Thanks to its natural strong fluorescence performance, 3-Phenylindole (CAS 1504-16-1) can be used to prepare organic fluorescent probes for biological cell imaging, ion detection and environmental pollutant analysis. It has low biological toxicity and high fluorescence quantum yield, adapting to biochemical detection research scenarios. 4. Organic Synthesis Building Block: It can undergo electrophilic substitution, Suzuki coupling, N-alkylation and other reactions to derive various multi-substituted indole compounds. It is an indispensable fragment for custom synthesis of complex nitrogen-containing heterocyclic molecules in organic chemistry R&D.

≥98% (HPLC/GC)

C14H11N

193.24

2 years under proper storage

White to off-white crystalline powder

Electronic Grade, Pharmaceutical Intermediate Grade, Laboratory Reagent Grade, Organic Synthesis Grade

1.156±0.06 g/cm3 at 25 °C

109 °C

394.0±11.0 °C at 760 mmHg