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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6O2
Molecular Weight 98.0999
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3-CYCLOPENTANEDIONE

SMILES

O=C1CCC(=O)C1

InChI

InChIKey=LOGSONSNCYTHPS-UHFFFAOYSA-N
InChI=1S/C5H6O2/c6-4-1-2-5(7)3-4/h1-3H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
A photochemical approach to pyridopyrroloquinoline derivatives as new potential anticancer agents.
2004 Jun
Gas-phase acidities of disubstituted methanes and of enols of carboxamides substituted by electron-withdrawing groups.
2004 Sep 3
Reactions of 1,2-bis(trimethylsilyloxy)cycloalkenes with the diethyl acetals of aldehydes.
2006 Jan 6
General strategy for the synthesis of B1 phytoprostanes, dinor isoprostanes, and analogs.
2007 Mar 2
Ruthenium/TFA-catalyzed coupling of activated secondary propargylic alcohols with cyclic 1,3-diones: furan versus pyran ring formation.
2008 Aug 1
2-(2,5-Dioxotetra-hydro-furan-3-yl)isoindoline-1,3-dione.
2008 Aug 6
Efficient total synthesis of novel bioactive microbial metabolites.
2008 Feb
Novel multicomponent reactions involving isoquinoline or phenanthridine and activated acetylenic ester in the presence of heterocyclic NH or 1,3-dicarbonyl compounds.
2008 May
Direct amino acid-catalyzed cascade biomimetic reductive alkylations: application to the asymmetric synthesis of Hajos-Parrish ketone analogues.
2008 Nov 21
Acylphloroglucinol, biyouyanagiol, biyouyanagin B, and related spiro-lactones from Hypericum chinense.
2009 Aug
Patents
Name Type Language
1,3-CYCLOPENTANEDIONE
Systematic Name English
NSC-364015
Code English
CYCLOPENTANE-1,3-DIONE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
1,3-Cyclopentanedione
Created by admin on Fri Dec 15 19:28:55 GMT 2023 , Edited by admin on Fri Dec 15 19:28:55 GMT 2023
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CAS
3859-41-4
Created by admin on Fri Dec 15 19:28:55 GMT 2023 , Edited by admin on Fri Dec 15 19:28:55 GMT 2023
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NSC
364015
Created by admin on Fri Dec 15 19:28:55 GMT 2023 , Edited by admin on Fri Dec 15 19:28:55 GMT 2023
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ECHA (EC/EINECS)
223-372-8
Created by admin on Fri Dec 15 19:28:55 GMT 2023 , Edited by admin on Fri Dec 15 19:28:55 GMT 2023
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PUBCHEM
77466
Created by admin on Fri Dec 15 19:28:55 GMT 2023 , Edited by admin on Fri Dec 15 19:28:55 GMT 2023
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EPA CompTox
DTXSID90191911
Created by admin on Fri Dec 15 19:28:55 GMT 2023 , Edited by admin on Fri Dec 15 19:28:55 GMT 2023
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FDA UNII
98107S5K06
Created by admin on Fri Dec 15 19:28:55 GMT 2023 , Edited by admin on Fri Dec 15 19:28:55 GMT 2023
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CHEBI
41456
Created by admin on Fri Dec 15 19:28:55 GMT 2023 , Edited by admin on Fri Dec 15 19:28:55 GMT 2023
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