| Identification | More | [Name]
6-Methylindole | [CAS]
3420-02-8 | [Synonyms]
6-METHYL-1H-INDOLE
6-METHYLINDOLE
AKOS JY2082811
Indole, 6-methyl-
6-Methyindole
6-Methylindole,98%
6-Metlylindole
1H-Indole,6-methyl-
6-METHYLINDOLE 99% | [Molecular Formula]
C9H9N | [MDL Number]
MFCD00005682 | [Molecular Weight]
131.17 | [MOL File]
3420-02-8.mol |
| Chemical Properties | Back Directory | [Appearance]
clear yellow to light brown liquid after melting | [Melting point ]
29-32°C | [Boiling point ]
112 °C/5 mmHg (lit.) | [density ]
1.059 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.607(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
0-6°C | [form ]
Liquid After Melting | [pka]
17.36±0.30(Predicted) | [color ]
Clear yellow to light brown | [Specific Gravity]
1.059 | [Water Solubility ]
Insoluble in water. | [Sensitive ]
Light Sensitive | [BRN ]
109708 | [InChIKey]
ONYNOPPOVKYGRS-UHFFFAOYSA-N | [LogP]
2.600 (est) | [CAS DataBase Reference]
3420-02-8(CAS DataBase Reference) | [NIST Chemistry Reference]
1H-Indole, 6-methyl-(3420-02-8) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
UN 3334 | [WGK Germany ]
3
| [Hazard Note ]
Light Sensitive/Irritant/Keep Cold | [HazardClass ]
IRRITANT, LIGHT SENSITIVE | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
clear yellow to light brown liquid after melting | [Uses]
6-Methylindole was used in the synthesis of benz[c,d]indol-3(1H)-one derivatives.
Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
Reactant for preparation of indole linked triazole derivatives as antifungal agents
Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes
Reactant for preparation of aminoguanidine derivatives of arylsulfonylacylindoles as antifungal agents
Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors
Reactant for preparation of arylsulfonylacetylindoles as anti-HIV-1 agents |
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