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Details

Stereochemistry ACHIRAL
Molecular Formula C12H9N3O2
Molecular Weight 227.2188
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 4-NITROAZOBENZENE

SMILES

[O-][N+](=O)C1=CC=C(C=C1)\N=N\C2=CC=CC=C2

InChI

InChIKey=TZTDJBMGPQLSLI-BUHFOSPRSA-N
InChI=1S/C12H9N3O2/c16-15(17)12-8-6-11(7-9-12)14-13-10-4-2-1-3-5-10/h1-9H/b14-13+

HIDE SMILES / InChI

Molecular Formula C12H9N3O2
Molecular Weight 227.2188
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
In situ raman spectroelectrochemistry of electron transfer between glassy carbon and a chemisorbed nitroazobenzene monolayer.
2002 Sep 11
Mono- and multilayer formation by diazonium reduction on carbon surfaces monitored with atomic force microscopy "scratching".
2003 Aug 1
Molecular rectification and conductance switching in carbon-based molecular junctions by structural rearrangement accompanying electron injection.
2003 Sep 3
In situ Raman spectroscopy of bias-induced structural changes in nitroazobenzene molecular electronic junctions.
2004 Dec 22
Characterization of carbon/nitroazobenzene/titanium molecular electronic junctions with photoelectron and Raman spectroscopy.
2004 Feb 15
Multilayer nitroazobenzene films covalently attached to carbon. An AFM and electrochemical study.
2005 May 12
Carbon/molecule/metal molecular electronic junctions: the importance of "contacts".
2006
Determination of the structure and orientation of organic molecules tethered to flat graphitic carbon by ATR-FT-IR and Raman spectroscopy.
2006 May 1
Resonance Raman spectroscopy and quantum-chemical calculations of push-pull molecules: 4-hydroxy-4'-nitroazobenzene and its anion.
2007 Dec 27
Normal and surface-enhanced Raman spectroscopy of nitroazobenzene submonolayers and multilayers on carbon and silver surfaces.
2007 Jun
Photoisomerization and thermal isomerization of arylazoimidazoles.
2007 Mar 1
Ultraviolet-visible spectroelectrochemistry of chemisorbed molecular layers on optically transparent carbon electrodes.
2007 Nov
(E)-2-{Eth-yl[4-(4-nitro-phenyl-diazen-yl)phen-yl]amino}ethyl anthracene-9-carboxyl-ate.
2008 Feb 15
Functionalization of glassy carbon with diazonium salts in ionic liquids.
2008 Jun 17
(E)-4-[(4-Nitro-phen-yl)diazen-yl]phenyl anthracene-9-carboxyl-ate.
2008 Nov 8
Molecular electronics using diazonium-derived adlayers on carbon with Cu top contacts: critical analysis of metal oxides and filaments.
2008 Sep 17
Optical interference effects in the design of substrates for surface-enhanced Raman spectroscopy.
2009 Feb
Synthesis, spectroscopy and photochemistry of nitro-azobenzene dyes bearing benzophenone parts.
2009 May
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:52:08 GMT 2023
Edited
by admin
on Fri Dec 15 17:52:08 GMT 2023
Record UNII
P8P9OZE3IH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-NITROAZOBENZENE
Systematic Name English
NSC-16043
Code English
DIAZENE, 1-(4-NITROPHENYL)-2-PHENYL-
Systematic Name English
AZOBENZENE, 4-NITRO-
Systematic Name English
DIAZENE, (4-NITROPHENYL)PHENYL-
Systematic Name English
NITROAZOBENZENE, 4-
Systematic Name English
P-NITROAZOBENZENE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID70870979
Created by admin on Fri Dec 15 17:52:08 GMT 2023 , Edited by admin on Fri Dec 15 17:52:08 GMT 2023
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NSC
16043
Created by admin on Fri Dec 15 17:52:08 GMT 2023 , Edited by admin on Fri Dec 15 17:52:08 GMT 2023
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ECHA (EC/EINECS)
219-656-6
Created by admin on Fri Dec 15 17:52:08 GMT 2023 , Edited by admin on Fri Dec 15 17:52:08 GMT 2023
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FDA UNII
P8P9OZE3IH
Created by admin on Fri Dec 15 17:52:08 GMT 2023 , Edited by admin on Fri Dec 15 17:52:08 GMT 2023
PRIMARY
CAS
2491-52-3
Created by admin on Fri Dec 15 17:52:08 GMT 2023 , Edited by admin on Fri Dec 15 17:52:08 GMT 2023
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PUBCHEM
17222
Created by admin on Fri Dec 15 17:52:08 GMT 2023 , Edited by admin on Fri Dec 15 17:52:08 GMT 2023
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