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Details

Stereochemistry ACHIRAL
Molecular Formula C10H4N2O4
Molecular Weight 216.1498
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PYROMELLITIC ACID DIIMIDE

SMILES

O=C1NC(=O)C2=CC3=C(C=C12)C(=O)NC3=O

InChI

InChIKey=UGQZLDXDWSPAOM-UHFFFAOYSA-N
InChI=1S/C10H4N2O4/c13-7-3-1-4-6(10(16)12-8(4)14)2-5(3)9(15)11-7/h1-2H,(H,11,13,15)(H,12,14,16)

HIDE SMILES / InChI

Molecular Formula C10H4N2O4
Molecular Weight 216.1498
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Enhanced hopping conductivity in low band gap donor-acceptor molecular wires Up to 20 nm in length.
2010-11-17
Mono- and bidentate imidates of five-coordinate nickel(II) with macrocyclic ligands: spectroscopic and photophysical properties.
2010-06-28
Excitation-wavelength-dependent photoluminescence of a pyromellitic diimide nanowire network.
2010-03-21
Tailoring bicomponent supramolecular nanoporous networks: phase segregation, polymorphism, and glasses at the solid-liquid interface.
2009-09-16
2,2'-(1,3,5,7-Tetra-oxo-1,2,3,5,6,7-hexa-hydro-pyrrolo[3,4-f]isoindole-2,6-di-yl)diacetic acid N,N-dimethyl-formamide disolvate.
2009-09-09
Electron transfer in the supramolecular donor-acceptor dyad of zinc porphycene.
2009-04-09
Electron transfer from the S1 and S2 states of pentacoordinated tetrapyrrole macrocycles to pyromellitic diimide as an axial ligand.
2007-11-15
Selective templated complexation of a cylindrical macrotricyclic host with neutral guests: three cation-controlled switchable processes.
2007-09-14
Interaction of pyromellitic diimide derivatives with beta-cyclodextrin and anthracene-appended beta-cyclodextrin: rim binding vs inclusion complexation.
2007-07-05
An anthracene-appended beta-cyclodextrin-based dyad: study of self-assembly and photoinduced electron-transfer processes.
2007
Metallomacrocycles that incorporate cofacially aligned diimide units.
2006-11-20
Supramolecular assemblies and redox modulation of pyromellitic diimide-based cyclophane via noncovalent interactions with naphthol.
2006-06-23
Doublet-quartet conversion in negative ions as a possible mechanism of the electron autodetachment delay.
2006
Controllable donor-acceptor neutral [2]rotaxanes.
2004-12-03
Switchable neutral bistable rotaxanes.
2004-08-18
Interrogating conformationally dependent electron-transfer dynamics via ultrafast visible pump/IR probe spectroscopy.
2004-03-10
Selective rearrangements of quadruply hydrogen-bonded dimer driven by donor-acceptor interaction.
2003-06-16
Vertical ionisation potentials of a number of crown ethers from charge transfer bands of their EDA complexes.
2002-11
Novel chiral pyromellitdiimide (1,2,4,5-benzenetetracarboxydiimide) dimers and trimers: exploring their structure, electronic transitions, and exciton coupling.
2002-06-03
Effect of antibiotics, 2-bromoethanesulfonic acid and pyromellitic diimide on methanogenesis in rumen ciliate cultures in vitro.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:56:01 GMT 2025
Edited
by admin
on Mon Mar 31 19:56:01 GMT 2025
Record UNII
32XA0W314G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-55160
Preferred Name English
PYROMELLITIC ACID DIIMIDE
Common Name English
1,2,4,5-BENZENETETRACARBOXYLIC 1,2:4,5-DIIMIDE
Systematic Name English
1,2,4,5-BENZENETETRACARBOXYLIC ACID DIIMIDE
Systematic Name English
PYROMELLITIC DIIMIDE
Common Name English
PYROMELLITIMIDE
Common Name English
BENZO(1,2-C:4,5-C')DIPYRROLE-1,3,5,7(2H,6H)-TETRONE
Systematic Name English
Code System Code Type Description
FDA UNII
32XA0W314G
Created by admin on Mon Mar 31 19:56:01 GMT 2025 , Edited by admin on Mon Mar 31 19:56:01 GMT 2025
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PUBCHEM
75696
Created by admin on Mon Mar 31 19:56:01 GMT 2025 , Edited by admin on Mon Mar 31 19:56:01 GMT 2025
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CAS
2550-73-4
Created by admin on Mon Mar 31 19:56:01 GMT 2025 , Edited by admin on Mon Mar 31 19:56:01 GMT 2025
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ECHA (EC/EINECS)
219-852-1
Created by admin on Mon Mar 31 19:56:01 GMT 2025 , Edited by admin on Mon Mar 31 19:56:01 GMT 2025
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NSC
55160
Created by admin on Mon Mar 31 19:56:01 GMT 2025 , Edited by admin on Mon Mar 31 19:56:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID4062515
Created by admin on Mon Mar 31 19:56:01 GMT 2025 , Edited by admin on Mon Mar 31 19:56:01 GMT 2025
PRIMARY