Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

5-Methylindole

From Wikipedia, the free encyclopedia
5-Methylindole[1]
Skeletal formula of 5-methylindole
Ball-and-stick model of the 5-methylindole molecule
Names
IUPAC name
5-Methyl-1H-indole
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.009.456 Edit this at Wikidata
UNII
  • InChI=1S/C9H9N/c1-7-2-3-9-8(6-7)4-5-10-9/h2-6,10H,1H3 checkY
    Key: YPKBCLZFIYBSHK-UHFFFAOYSA-N checkY
  • InChI=1/C9H9N/c1-7-2-3-9-8(6-7)4-5-10-9/h2-6,10H,1H3
    Key: YPKBCLZFIYBSHK-UHFFFAOYAI
  • CC1=CC2=C(C=C1)NC=C2
  • Cc1ccc2c(c1)cc[nH]2
Properties
C9H9N
Molar mass 131.178 g·mol−1
Melting point 58 to 61 °C (136 to 142 °F; 331 to 334 K)
Related compounds
Related compounds
Indole
1-Methylindole
2-Methylindole (methylketol)
Skatole (3-methylindole)
4-Methylindole
6-Methylindole
7-Methylindole
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X markN verify (what is checkYX markN ?)

5-Methylindole is an irritating organic compound with chemical formula C9H9N. 5-Methylindole is used as an intermediate in the synthesis of compounds with a variety of pharmacological properties, such as staurosporine-like bisindole inhibitors of protein kinases.[2]

References

[edit]
  1. 5-Methylindole ChemExper Chemical Directory. Accessed 1 September 2005.
  2. Hanns Martin Kaiser; Wei Fun Lo; Abdol Majid Riahi; Anke Spannenberg; Matthias Beller & Man Kin Tse (2006). "New Synthetic Protocols for the Preparation of Unsymmetrical Bisindoles". Org. Lett. 8 (25): 5761–5764. doi:10.1021/ol062338p. PMID 17134266.