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Details

Stereochemistry ACHIRAL
Molecular Formula C10H15N
Molecular Weight 149.2328
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIETHYLANILINE

SMILES

CCN(CC)C1=CC=CC=C1

InChI

InChIKey=GGSUCNLOZRCGPQ-UHFFFAOYSA-N
InChI=1S/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C10H15N
Molecular Weight 149.2328
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
5-amino-4-(4-diethylaminophenyl)-2-(4-hydroxyphenyl)-7-(pyrrolidin-1-yl)-1,6-naphthyridine-8-carbonitrile.
2001 Jun
Studies in sigmatropic rearrangement: synthesis of a [6,6]pyranothiopyran ring system by sequential claisen rearrangement and pyridine hydrotribromide mediated regioselective "6-Endo" cyclization.
2002 Aug 8
Concise synthesis and transannular inverse electron demand Diels-Alder reaction of [3](3,6)pyridazino[3](1,3)indolophane. Rapid access to a pentacyclic indoloid system.
2002 Jan 10
Photodegradation of acetochlor in water and UV photoproducts identified by mass spectrometry.
2003 Nov
Overtone spectra of aniline derivatives.
2004 Jan
The first total synthesis of kwakhurin, a characteristic component of a rejuvenating plant, "kwao keur": toward an efficient synthetic route to phytoestrogenic isoflavones.
2005 Feb 21
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Understanding reactivity patterns of the dialkylaniline radical cation.
2006 Dec 22
Properties of excited ketyl radicals of benzophenone analogues affected by the size and electronic character of the aromatic ring systems.
2006 Feb 8
Further evidence of an inverted region in proton transfer within the benzophenone/substituted aniline contact radical ion pairs; importance of vibrational reorganization energy.
2006 May 25
1,6,6-Trimethyl-1H-chromeno[6,7-d]thia-zol-2(6H)-one.
2008 Apr 23
Fourier-transform infrared and optical absorption spectra of 4-tricyanovinyl-N,N-diethylaniline thin films.
2008 Jan
The electrochemical grafting of a mixture of substituted phenyl groups at a glassy carbon electrode surface.
2008 Jun 2
Highly enantioselective oxazaborolidine-catalyzed reduction of 1,3-dicarbonyl compounds: role of the additive diethylaniline.
2009 Apr 2
Fullerene derivatives functionalized with diethylamino-substituted conjugated oligomers: synthesis and photoinduced electron transfer.
2009 Sep 7
Biodegradation of N,N diethylaniline in a contaminated aquifer: Laboratory- and field-scale evidences.
2010 Apr
Photoinduced electron transfer in photorobust coumarins linked with electron donors affording long lifetimes of triplet charge-separated states.
2010 Aug 23
Optical, redox, and DNA-binding properties of phenanthridinium chromophores: elucidating the role of the phenyl substituent for fluorescence enhancement of ethidium in the presence of DNA.
2010 Mar 15
2-{[4-(Diethyl-amino)-phen-yl]imino-methyl}-4,6-diiodo-phenol.
2010 Nov 6
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:08:37 GMT 2023
Edited
by admin
on Fri Dec 15 19:08:37 GMT 2023
Record UNII
1WR1HJ2PGW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIETHYLANILINE
MI  
Systematic Name English
N,N-DIETHYLANILINE [HSDB]
Common Name English
ANILINE, N,N-DIETHYL-
Systematic Name English
BENZENAMINE, N,N-DIETHYL-
Systematic Name English
DIETHYL ANILINE, N,N-
Common Name English
N,N-DIETHYLANILINE
HSDB  
Systematic Name English
N,N-DIETHYLBENZENAMINE
Systematic Name English
DIETHYLANILINE [MI]
Common Name English
NSC-7205
Code English
Code System Code Type Description
CAS
91-66-7
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-088-8
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY
WIKIPEDIA
DIETHYLANILINE
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY
PUBCHEM
7061
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID8021800
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY
HSDB
1639
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY
MERCK INDEX
m4395
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY Merck Index
NSC
7205
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY
FDA UNII
1WR1HJ2PGW
Created by admin on Fri Dec 15 19:08:37 GMT 2023 , Edited by admin on Fri Dec 15 19:08:37 GMT 2023
PRIMARY