| Identification | More | [Name]
1-Methyl-2-phenylindole | [CAS]
3558-24-5 | [Synonyms]
1-METHYL-2-PHENYL-1H-INDOLE
1-METHYL-2-PHENYLINDOLE
N-METHYL-2-PHENYLINDOLE
1-methyl-2-phenyl-1h-indol
1-Methyl-2-Phenylindol
1-METHYL-2-PHENYLINDOLE 99+%
1H-Indole, 1-methyl-2-phenyl-
2-Phenyl-N-methylindole
2-Phenyl-1-methyl-1H-indole | [EINECS(EC#)]
222-618-1 | [Molecular Formula]
C15H13N | [MDL Number]
MFCD00022892 | [Molecular Weight]
207.27 | [MOL File]
3558-24-5.mol |
| Chemical Properties | Back Directory | [Appearance]
WHITE TO LIGHT GREEN-TAN CRYSTALS OR CRYST. POWDER | [Melting point ]
98-100 °C (lit.) | [Boiling point ]
336.3°C (rough estimate) | [density ]
1.0880 (rough estimate) | [refractive index ]
1.5720 (estimate) | [storage temp. ]
2-8°C | [form ]
powder to crystal | [color ]
White to Light yellow | [Detection Methods]
HPLC | [BRN ]
148770 | [InChI]
InChI=1S/C15H13N/c1-16-14-10-6-5-9-13(14)11-15(16)12-7-3-2-4-8-12/h2-11H,1H3 | [InChIKey]
SFWZZSXCWQTORH-UHFFFAOYSA-N | [SMILES]
N1(C)C2=C(C=CC=C2)C=C1C1=CC=CC=C1 | [CAS DataBase Reference]
3558-24-5(CAS DataBase Reference) | [EPA Substance Registry System]
3558-24-5(EPA Substance) |
| Hazard Information | Back Directory | [Chemical Properties]
WHITE TO LIGHT GREEN-TAN CRYSTALS OR CRYST. POWDER | [Uses]
Reactant for preparation of:
- Cyano indoles
- Difluorohydroxy indoles
Reactant for:
- Carboxylation of indoles
- Allylation of indoles
- Formylation of indoles
- Nitrosylation of indoles
| [Synthesis Reference(s)]
Tetrahedron Letters, 34, p. 2059, 1993 DOI: 10.1016/S0040-4039(00)60345-3 | [General Description]
Reaction of 1-methyl-2-phenylindole with nitrogen dioxide or with nitrous acid (NaNO2-CH3COOH) in benzene has been studied. 1-Methyl-2-phenylindole is reported to react with malondialdehyde (MDA) and 4-hydroxyalkenals to afford a stable chromophore with intense maximal absorbance at 586nm. | [References]
[1] Jason W. Johnston. “Evaluation of the 1-methyl-2-phenylindole colorimetric assay for aldehydic lipid peroxidation products in plants: Malondialdehyde and 4-hydroxynonenal.” Plant Physiology and Biochemistry 45 2 (2007): Pages 108-112.
[2] Dominique Gérard-Monnier. “Reactions of 1-Methyl-2-phenylindole with Malondialdehyde and 4-Hydroxyalkenals. Analytical Applications to a Colorimetric Assay of Lipid Peroxidation.” Chemical Research in Toxicology 11 10 (1998): 1176–1183.
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