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Details

Stereochemistry ACHIRAL
Molecular Formula C9H8O
Molecular Weight 132.1592
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2H-INDEN-2-ONE, 1,3-DIHYDRO-

SMILES

O=C1CC2=CC=CC=C2C1

InChI

InChIKey=UMJJFEIKYGFCAT-UHFFFAOYSA-N
InChI=1S/C9H8O/c10-9-5-7-3-1-2-4-8(7)6-9/h1-4H,5-6H2

HIDE SMILES / InChI

Molecular Formula C9H8O
Molecular Weight 132.1592
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Calculation of the vibrationally resolved, circularly polarized luminescence of d-camphorquinone and (S,S)-trans-beta-hydrindanone.
2010-08-02
Diastereoisomers of 2-benzyl-2, 3-dihydro-2-(1H-inden-2-yl)-1H-inden-1-ol: potential anti-inflammatory agents.
2009-10-15
Bacterial degradation of aromatic compounds.
2009-01
Calorimetric and computational study of indanones.
2007-11-01
Experimental study on the thermal oxidation of 2-chlorophenol in air over the temperature range 450-900 degrees C.
2006-03
Aromatic and aliphatic hydrocarbon consumption and transformation by the styrene degrading strain Pseudomonas putida CA-3.
2005-08-15
Lipoprotein mutation accelerates substrate permeability-limited toluene dioxygenase-catalyzed reaction.
2005-06-04
Syntheses of 2-substituted indoles and fused indoles by photostimulated reactions of o-iodoanilines with carbanions by the SRN1 mechanism.
2003-04-04
Synthesis of 2-indanones via [4 + 1] annulation reactions of (trialkylsilyl)arylketenes.
2002-07-25
New metabolites in the degradation of fluorene by Arthrobacter sp. strain F101.
1997-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:01:31 GMT 2025
Edited
by admin
on Mon Mar 31 19:01:31 GMT 2025
Record UNII
0I79N673DE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2H-INDEN-2-ONE, 1,3-DIHYDRO-
Systematic Name English
1,3-DIHYDRO-2H-INDEN-2-ONE
Preferred Name English
Code System Code Type Description
ECHA (EC/EINECS)
210-410-3
Created by admin on Mon Mar 31 19:01:31 GMT 2025 , Edited by admin on Mon Mar 31 19:01:31 GMT 2025
PRIMARY
CHEBI
27930
Created by admin on Mon Mar 31 19:01:31 GMT 2025 , Edited by admin on Mon Mar 31 19:01:31 GMT 2025
PRIMARY
FDA UNII
0I79N673DE
Created by admin on Mon Mar 31 19:01:31 GMT 2025 , Edited by admin on Mon Mar 31 19:01:31 GMT 2025
PRIMARY
EPA CompTox
DTXSID7052288
Created by admin on Mon Mar 31 19:01:31 GMT 2025 , Edited by admin on Mon Mar 31 19:01:31 GMT 2025
PRIMARY
CAS
615-13-4
Created by admin on Mon Mar 31 19:01:31 GMT 2025 , Edited by admin on Mon Mar 31 19:01:31 GMT 2025
PRIMARY
PUBCHEM
11983
Created by admin on Mon Mar 31 19:01:31 GMT 2025 , Edited by admin on Mon Mar 31 19:01:31 GMT 2025
PRIMARY