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Details

Stereochemistry ACHIRAL
Molecular Formula C9H6O2
Molecular Weight 146.1427
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3-INDANDIONE

SMILES

O=C1CC(=O)C2=C1C=CC=C2

InChI

InChIKey=UHKAJLSKXBADFT-UHFFFAOYSA-N
InChI=1S/C9H6O2/c10-8-5-9(11)7-4-2-1-3-6(7)8/h1-4H,5H2

HIDE SMILES / InChI

Molecular Formula C9H6O2
Molecular Weight 146.1427
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A convenient ultrasound-promoted regioselective synthesis of fused polycyclic 4-aryl-3-methyl-4,7-dihydro-1H-pyrazolo[3,4-b]pyridines.
2010-02
The E3 ubiquitin-ligase Bmi1/Ring1A controls the proteasomal degradation of Top2alpha cleavage complex - a potentially new drug target.
2009-12-01
4'-Ferrocenyl-1'-methylacenapthylene-1-spiro-2'-pyrrolidine-3'-spiro-2''-indane-2,1'',3''(1H)-trione.
2009-11-25
Strapped calix[4]pyrroles bearing a 1,3-indanedione at a beta-pyrrolic position: chemodosimeters for the cyanide anion.
2009-08-20
Organic synthesis in water: a green protocol for the synthesis of 2-(cyclohexylamino)-3- aryl- indeno[1,2-b]furan-4-ones.
2009-08
Selective formation of spiro dihydrofurans and cyclopropanes through unexpected reaction of aldehydes with 1,3-dicarbonyl compounds.
2009-06-04
Design and microwave-assisted synthesis of naphtho[2,3-f]quinoline derivatives and their luminescent properties.
2009-03-09
Chemical substructures that enrich for biological activity.
2008-11-01
Synthesis and antimicrobial study of novel 1-aryl-2-oxo-indano[3,2-d]pyrido/pyrimido[1,2-b]pyrimidines.
2008-07
2-(4,5,6,7,8,9-Hexahydro-6a-aza-phenyl-en-2-ylmethyl-ene)indan-1,3-dione.
2008-06-07
An efficient synthesis of pyrido[2,3-d]pyrimidine derivatives and related compounds under ultrasound irradiation without catalyst.
2008-03
Three-component synthesis and anticancer evaluation of polycyclic indenopyridines lead to the discovery of a novel indenoheterocycle with potent apoptosis inducing properties.
2007-12-07
Calorimetric and computational study of indanones.
2007-11-01
Synthesis and molluscicidal activity of new chromene and pyrano[2,3-c]pyrazole derivatives.
2007-10
Rh(I)-catalyzed carbonylative cyclization reactions of alkynes with 2-bromophenylboronic acids leading to indenones.
2007-05-02
A green method for the electroorganic synthesis of new 1,3-Indandione derivatives.
2006-10
Uptake and UV-photooxidation of gas-phase PAHs on the surface of atmospheric water films. 1. Naphthalene.
2006-07-27
Three-component synthesis of functionalized 5-oxo-4,5-dihydroindeno[1,2-b]pyrans.
2006-05
Long-chain 3-acyl-4-hydroxycoumarins: structure and antibacterial activity.
2006-03
1,3-indane-based chromogenic calixpyrroles with push-pull chromophores: synthesis and anion sensing.
2006-02-02
The genetic basis of resistance to anticoagulants in rodents.
2005-08
Gas-phase acidities of disubstituted methanes and of enols of carboxamides substituted by electron-withdrawing groups.
2004-09-03
Direct organocatalytic asymmetric heterodomino reactions: the Knoevenagel/Diels-Alder/epimerization sequence for the highly diastereoselective synthesis of symmetrical and nonsymmetrical synthons of benzoannelated centropolyquinanes.
2004-09-03
Highly regio- and chemoselective palladium-catalyzed propargylallylation of activated olefins: a novel route to 1,7-enyne derivatives.
2004-06-11
Synthesis and pharmacological properties of sulfur derivatives of indane-1,3-dione.
2003-02-27
Reactions of enols of amides with diazomethane.
2002-10-04
Structural assignment of isomeric 2-(2-quinolinyl)-1H-indene-1,3(2H)-dione mono- and disulfonic acids by liquid chromatography electrospray and atmospheric pressure chemical ionization tandem mass spectrometry.
2001-09
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:49:57 GMT 2025
Edited
by admin
on Mon Mar 31 18:49:57 GMT 2025
Record UNII
4DJN7YG35G
Record Status Validated (UNII)
Record Version
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Name Type Language
1,3-INDANDIONE
Systematic Name English
J7.003C
Preferred Name English
INDANEDIONE-1,3
Common Name English
1,3-HYDRINDENDIONE
Common Name English
2,3-DIHYDRO-1,3-DIOXO-1H-INDENE
Systematic Name English
1,3-DIOXOBENZOCYCLOPENTANE
Systematic Name English
2,3-DIHYDRO-1H-INDENE-1,3-DIONE
Systematic Name English
1H-INDENE-1,3(2H)-DIONE
Systematic Name English
2H-INDENE-1,3-DIONE
Systematic Name English
1,3-INDANONE
Common Name English
NSC-26329
Code English
NSC-6312
Code English
INDANDIONE
Systematic Name English
3-OXO-1-INDANONE
Systematic Name English
1,3-INDANEDIONE
Systematic Name English
INDAN-1,3-DIONE
Systematic Name English
2-HYDROCYCLOPENTA(1,2-A)BENZENE-1,3-DIONE
Systematic Name English
1,3-DIKETOHYDRINDENE
Common Name English
INDENE-1,3(2H)-DIONE
Systematic Name English
INDANDIONE, 1,3-
Systematic Name English
Code System Code Type Description
NSC
6312
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-109-7
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY
CHEBI
78877
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY
PUBCHEM
11815
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY
FDA UNII
4DJN7YG35G
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY
NSC
26329
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY
CAS
606-23-5
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY
EPA CompTox
DTXSID2060547
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY
WIKIPEDIA
1,3-Indandione
Created by admin on Mon Mar 31 18:49:57 GMT 2025 , Edited by admin on Mon Mar 31 18:49:57 GMT 2025
PRIMARY