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Details

Stereochemistry ACHIRAL
Molecular Formula C9H9N
Molecular Weight 131.1745
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-METHYLINDOLE

SMILES

CC1=CC2=C(N1)C=CC=C2

InChI

InChIKey=BHNHHSOHWZKFOX-UHFFFAOYSA-N
InChI=1S/C9H9N/c1-7-6-8-4-2-3-5-9(8)10-7/h2-6,10H,1H3

HIDE SMILES / InChI

Molecular Formula C9H9N
Molecular Weight 131.1745
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
DNA mediated charge transport: characterization of a DNA radical localized at an artificial nucleic acid base.
2002 Aug 7
Primary electron-transfer dynamics in 2-phenylindole-9-cyanoanthracene system. A comparative study with 2-methylindole.
2004 Jul
Adsorption of indole and 2-methylindole on ligand-exchange matrix.
2004 Oct 1
Synthesis and pharmacological evaluation of peptide-mimetic protease-activated receptor-1 antagonists containing novel heterocyclic scaffolds.
2008 Jun 1
An odorant receptor from the southern house mosquito Culex pipiens quinquefasciatus sensitive to oviposition attractants.
2010 Apr 8
The Anopheles gambiae odorant binding protein 1 (AgamOBP1) mediates indole recognition in the antennae of female mosquitoes.
2010 Mar 1
Cytosolic action of phytochelatin synthase.
2010 May
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:38:03 UTC 2023
Edited
by admin
on Fri Dec 15 18:38:03 UTC 2023
Record UNII
I7CN58827I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-METHYLINDOLE
Systematic Name English
NSC-7514
Code English
2-METHYL-1H-INDOLE
Systematic Name English
INDOLE, 2-METHYL-
Systematic Name English
1H-INDOLE, 2-METHYL-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
2-METHYLINDOLE
Created by admin on Fri Dec 15 18:38:03 UTC 2023 , Edited by admin on Fri Dec 15 18:38:03 UTC 2023
PRIMARY
CAS
95-20-5
Created by admin on Fri Dec 15 18:38:03 UTC 2023 , Edited by admin on Fri Dec 15 18:38:03 UTC 2023
PRIMARY
EPA CompTox
DTXSID5059117
Created by admin on Fri Dec 15 18:38:03 UTC 2023 , Edited by admin on Fri Dec 15 18:38:03 UTC 2023
PRIMARY
CHEBI
49402
Created by admin on Fri Dec 15 18:38:03 UTC 2023 , Edited by admin on Fri Dec 15 18:38:03 UTC 2023
PRIMARY
PUBCHEM
7224
Created by admin on Fri Dec 15 18:38:03 UTC 2023 , Edited by admin on Fri Dec 15 18:38:03 UTC 2023
PRIMARY
FDA UNII
I7CN58827I
Created by admin on Fri Dec 15 18:38:03 UTC 2023 , Edited by admin on Fri Dec 15 18:38:03 UTC 2023
PRIMARY
ECHA (EC/EINECS)
202-398-3
Created by admin on Fri Dec 15 18:38:03 UTC 2023 , Edited by admin on Fri Dec 15 18:38:03 UTC 2023
PRIMARY
NSC
7514
Created by admin on Fri Dec 15 18:38:03 UTC 2023 , Edited by admin on Fri Dec 15 18:38:03 UTC 2023
PRIMARY