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Details

Stereochemistry ACHIRAL
Molecular Formula C14H13N
Molecular Weight 195.2597
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 9-ETHYLCARBAZOLE

SMILES

CCN1C2=C(C=CC=C2)C3=C1C=CC=C3

InChI

InChIKey=PLAZXGNBGZYJSA-UHFFFAOYSA-N
InChI=1S/C14H13N/c1-2-15-13-9-5-3-7-11(13)12-8-4-6-10-14(12)15/h3-10H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C14H13N
Molecular Weight 195.2597
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
9-Ethyl-3,6-bis-(5-iodo-2-thien-yl)-9H-carbazole.
2010-02-10
Experimental and theoretical study of a new carbazole derivative having terminal benzimidazole rings.
2010-02
Electropolymerization of N-ethylcarbazole on single walled carbon nanotubes-cyclic voltammetry, raman and FTIR studies.
2009-10
Synthesis and spectral characteristics of two novel intramolecular charge transfer fluorescent dyes.
2009-03-15
Effect of latanoprost and timolol on the histopathology of the human conjunctiva.
2009-02
9-Ethyl-3,6-diformyl-9H-carbazole.
2008-06-19
Ring contracting sulfur extrusion from oxidized phenothiazine ring systems.
2008-06-12
Magnetic field effect on fluorescence in a mixture of N-ethylcarbazole and dimethyl terephthalate in a polymer film in the presence of electric fields.
2008-05-15
Vertical and directional insertion of helical peptide into lipid bilayer membrane.
2007-06-19
Charge-transfer complex formation between p-chloranil and 1,n-dicarbazolylalkanes.
2007-04
Photoinduced charge separation and charge recombination in [60]fullerene-ethylcarbazole and [60]fullerene-triphenylamines in polar solvents.
2005-06-02
Cyclohexyl-octahydro-pyrrolo[1,2-a]pyrazine-based inhibitors of human N-myristoyltransferase-1.
2004-04
Evaluation of the parameters of 1:1 charge transfer complexes from spectrophotometric data by non-linear numerical method.
2002-11
Three polar derivatives of N-ethylcarbazole: materials for optical applications.
2002-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:50:39 GMT 2025
Edited
by admin
on Mon Mar 31 22:50:39 GMT 2025
Record UNII
6AK165L0RO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
9-ETHYLCARBAZOLE
Systematic Name English
NSC-60585
Preferred Name English
9H-CARBAZOLE, 9-ETHYL-
Systematic Name English
CARBAZOLE, 9-ETHYL-
Systematic Name English
N-ETHYLCARBAZOLE
Systematic Name English
9-ETHYL-9H-CARBAZOLE
Systematic Name English
Code System Code Type Description
FDA UNII
6AK165L0RO
Created by admin on Mon Mar 31 22:50:39 GMT 2025 , Edited by admin on Mon Mar 31 22:50:39 GMT 2025
PRIMARY
PUBCHEM
6836
Created by admin on Mon Mar 31 22:50:39 GMT 2025 , Edited by admin on Mon Mar 31 22:50:39 GMT 2025
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NSC
60585
Created by admin on Mon Mar 31 22:50:39 GMT 2025 , Edited by admin on Mon Mar 31 22:50:39 GMT 2025
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ECHA (EC/EINECS)
201-660-4
Created by admin on Mon Mar 31 22:50:39 GMT 2025 , Edited by admin on Mon Mar 31 22:50:39 GMT 2025
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EPA CompTox
DTXSID1052585
Created by admin on Mon Mar 31 22:50:39 GMT 2025 , Edited by admin on Mon Mar 31 22:50:39 GMT 2025
PRIMARY
CAS
86-28-2
Created by admin on Mon Mar 31 22:50:39 GMT 2025 , Edited by admin on Mon Mar 31 22:50:39 GMT 2025
PRIMARY