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3420-02-8 - 6-Methylindole, 98% - L17509 - Alfa Aesar

L17509 6-Methylindole, 98%

CAS-Nummer
3420-02-8
Synonyme

Größe Preis ($) Menge Verfügbarkeit
250mg 54,50
1g 152,00
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6-Methylindole, 98%

MDL
MFCD00005682

Chemische Eigenschaften

Formel
C9H9N
Molmasse
131.18
Schmelzpunkt
29-32°
Siedepunkt
112°/5mm
Flammpunkt
>110°(230°F)
Dichte
1.059
Brechungsindex
1.6071
Sensitivität
Light Sensitive
Löslichkeit
Insoluble in water.

Anwendungen

It is a 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. 6-Methylindole was used in the synthesis of benz[c,d]indol-3(1H)-one derivatives.

Bemerkungen

Moisture and light sensitive. Store in dry condition. Keep away from active metals, bases, oxidizing agents and heat.

Literaturverweise

H. R. Snyder.; Frederick J. Pilgrim. A Synthesis of 6-Methylindole and dl-6-Methyltryptophan.J. Am. Chem. Soc. 1948, 70 (11),3787-3788 .

Urs Hengartner.; Donald ValentineJr.; Katharine K. Johnson.; Mary Ellen Larscheid.; Foster Pigott.; Franz Scheidl.; John W. Scott.; Ruen C. Sun.; John M. Townsend.Synthesis of (R)-6-methyltryptophan via enantioselective catalytic hydrogenation. J. Org. Chem. 1979, 44 (22),3741-3747 .

Weitere Referenzen

Beilstein
109708
Harmonized Tariff Code
2933.99
TSCA
No

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