CAS 3469-20-3
:2,3-Diphenylindole
Description:
2,3-Diphenylindole is an organic compound characterized by its indole structure, which features two phenyl groups attached to the 2 and 3 positions of the indole ring. This compound typically appears as a solid at room temperature and is known for its relatively low solubility in water, but it can dissolve in organic solvents such as ethanol and chloroform. 2,3-Diphenylindole exhibits interesting photophysical properties, making it useful in various applications, including organic electronics and as a dye. Its molecular structure contributes to its stability and potential reactivity, particularly in the presence of electrophiles or under UV light. Additionally, it may exhibit fluorescence, which can be harnessed in analytical chemistry for detection purposes. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Overall, 2,3-Diphenylindole is a compound of interest in both academic research and industrial applications due to its unique properties.
Formula:C20H15N
InChI:InChI=1/C20H15N/c1-3-9-15(10-4-1)19-17-13-7-8-14-18(17)21-20(19)16-11-5-2-6-12-16/h1-14,21H
InChI key:InChIKey=GYGKJNGSQQORRG-UHFFFAOYSA-N
SMILES:C1(=C(NC=2C1=CC=CC2)C3=CC=CC=C3)C4=CC=CC=C4
Synonyms:- 1H-Indole, 2,3-diphenyl-
- 2,3-Diphenyl-1H-indole
- Indole, 2,3-diphenyl-
- NSC 17363
- 2,3-Diphenylindole
- isopropyl 2,3-diphenyl-1H-indole-1-carboxylate
- 3-DIPHENYLINDOLE
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Found 5 products.
2,3-Diphenylindole
CAS:Purity:95.0%Color and Shape:Solid, No data available.Molecular weight:269.346984863281252,3-Diphenyl-1H-indole
CAS:Formula:C20H15NPurity:>98.0%(HPLC)(N)Color and Shape:White to Light yellow powder to crystalMolecular weight:269.352,3-Diphenylindole
CAS:<p>2,3-Diphenylindole is a benzyl-substituted indole with the chemical formula C14H10N2. It is an organic compound that was first synthesized in 1887 by German chemist Adolf von Baeyer. 2,3-Diphenylindole was one of the first aromatic compounds to be synthesized from benzene. The synthesis of 2,3-diphenylindole involves Friedel-Crafts reactions with amines and azides. Benzyl groups can be cleaved from the molecule under UV irradiation or by treatment with carboxylic acid. Reaction yields are increased when primary amines are used as the starting material, since they are more reactive than secondary amines or tertiary amines.</p>Formula:C20H15NPurity:Min. 95%Molecular weight:269.34 g/mol




