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

L17509 6-Methylindole, 98%

CAS Number
3420-02-8
Synonyms

Size Price ($) Quantity Availability
250mg 54.50
1g 152.00
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6-Methylindole, 98%

MDL
MFCD00005682

Chemical Properties

Formula
C9H9N
Formula Weight
131.18
Melting point
29-32°
Boiling Point
112°/5mm
Flash Point
>110°(230°F)
Density
1.059
Refractive Index
1.6071
Sensitivity
Light Sensitive
Solubility
Insoluble in water.

Applications

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.

Notes

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

Literature References

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 .

Other References

Beilstein
109708
Harmonized Tariff Code
2933.99
TSCA
No

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