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Name | 2-(4-Methoxyphenyl)-1H-Indole |
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Synonyms | 1H-INDOLE,2-(4-METHOXYPHENYL)-; 2-(4-Methoxyphenyl)-1H-indole; 4-(1H-indol-2-yl)phenyl methyl ether |
Molecular Structure | ![]() |
Molecular Formula | C15H13NO |
Molecular Weight | 223.27 |
CAS Registry Number | 63834-14-0 |
SMILES | COC1=CC=C(C=C1)C2=CC3=CC=CC=C3N2 |
InChI | 1S/C15H13NO/c1-17-13-8-6-11(7-9-13)15-10-12-4-2-3-5-14(12)16-15/h2-10,16H,1H3 |
InChIKey | BHCBPEBRFMLOND-UHFFFAOYSA-N |
Density | 1.2±0.1g/cm3 (Cal.) |
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Boiling point | 425.1±28.0°C at 760 mmHg (Cal.) |
Flash point | 153.4±14.3°C (Cal.) |
(1) | Ferdinand S. MelkonyanPresent address: Department of Chemistry, University of Illinois at Chicago, 845 W. Taylor St., Chicago, IL, 60607, USA. E-mail: fmelkon@uic.edu, Daniil E. Kuznetsov, Marina A. Y urovskaya and Alexander V. Karchava. One-pot synthesis of substituted indoles via titanium(iv) alkoxide mediated imine formation – copper-catalyzed N-arylation, RSC Advances, 2013, 3, 8388. |
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Market Analysis Reports |
List of Reports Available for 2-(4-Methoxyphenyl)-1H-Indole |