Misplaced Pages

7-Methylindole

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
(Redirected from 7-methylindole)
7-Methylindole
Skeletal formula of 7-methylindole
Ball-and-stick model of the 7-methylindole molecule
Names
Preferred IUPAC name 7-Methyl-1H-indole
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.012.064 Edit this at Wikidata
EC Number
  • 213-270-1
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C9H9N/c1-7-3-2-4-8-5-6-10-9(7)8/h2-6,10H,1H3Key: KGWPHCDTOLQQEP-UHFFFAOYSA-N
  • InChI=1/C9H9N/c1-7-3-2-4-8-5-6-10-9(7)8/h2-6,10H,1H3Key: KGWPHCDTOLQQEP-UHFFFAOYAX
SMILES
  • CC1=C2C(C=CN2)=CC=C1
  • Cc1cccc2c1cc2
Properties
Chemical formula C9H9N
Molar mass 131.178 g·mol
Hazards
GHS labelling:
Pictograms GHS07: Exclamation mark
Signal word Warning
Hazard statements H315, H319, H335
Precautionary statements P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

7-Methylindole is a mildly toxic off-white crystalline organic compound with chemical formula C9H9N.

Preparation

7-Methylindole can be prepared from 2,6-dimethylformanilide by reaction with potassium ethoxide.

Uses

7-Methylindole is used in the production of agricultural chemicals and pharmaceuticals.

See also

References

  1. Bass, K. C.; Nababsing, P. (1970). "7-Methylindole". Organic Preparations and Procedures. 2 (3): 221–222. doi:10.1080/00304947009458661.


Stub icon

This article about a heterocyclic compound is a stub. You can help Misplaced Pages by expanding it.

Categories: