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615-13-4,MFCD00003792
Catalog No.:AA003HDE
615-13-4 | 2-Indanone
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Purity
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Price(USD)
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5g
98%
in stock  
$8.00
- +
10g
98%
in stock  
$15.00
- +
25g
98%
in stock  
$25.00
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  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003HDE
Chemical Name:
2-Indanone
CAS Number:
615-13-4
Molecular Formula:
C9H8O
Molecular Weight:
132.1592
MDL Number:
MFCD00003792
IUPAC Name:
1,3-dihydroinden-2-one
InChI:
InChI=1S/C9H8O/c10-9-5-7-3-1-2-4-8(7)6-9/h1-4H,5-6H2
InChI Key:
UMJJFEIKYGFCAT-UHFFFAOYSA-N
SMILES:
O=C1Cc2c(C1)cccc2
EC Number:
210-410-3
UNII:
0I79N673DE
Properties
Computed Properties
 
Complexity:
135  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
132.058g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
132.162g/mol
Monoisotopic Mass:
132.058g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.3  

Synonyms
 
2-INDANONE 
615-13-4 
1,3-dihydroinden-2-one 
MFCD00003792 
BRN 0636550 
AI3-39163 
CHEMBL195557 
CHEBI:27930 
UMJJFEIKYGFCAT-UHFFFAOYSA-N 
0I79N673DE 
4-07-00-01002 (Beilstein Handbook Reference) 
2-Indanone, 97% 
Indan-2-one 
2-lndanone 
2-Oxoindane 
.beta.-Hydrindone 
indan-2-on 
2-Indanone; 
PubChem9653 
2-Indanone, 98% 
AC1L1YKX 
AC1Q6EFW 
ACMC-1BGA4 
1h-inden-2(3h)-one 
bmse000514 
1,3-dihydro-inden-2-one 
DSSTox_CID_30860 
DSSTox_GSID_52288 
SCHEMBL77106 
KSC352S6N 
DTXSID7052288 
CTK2F2966 
ZINC897211 
KS-000001VR 
1,3-Dihydro-2H-inden-2-one 
Tox21_304008 
AC-530 
ANW-33839 
BDBM50168003 
AKOS000120641 
ACN-030558 
CS-W020518 
MCULE-7616598839 
RP20002 
RTR-021188 
beta-Hydrindone 
TRA0068030 
NCGC00357223-01 
AJ-24270 
AK-78528 
AN-15736 
AS-11788 
BC214987 
CAS-615-13-4 
LS-81313 
SC-05757 
2H-Inden-2-one, 1,3-dihydro- 
SY001481 
ZB015129 
AB1003484 
DB-003899 
ST2408910 
TR-021188 
2-Indanone, Vetec(TM) reagent grade, 98% 
FT-0612646 
I0649 
ST51037957 
UNII-0I79N673DE 
TL80073601 
EN300-21015 
MFCD00003792 (98%) 
C07727 
M-4343 
A833275 
I14-0035 
W-105145 
F0001-1623 
InChI=1/C9H8O/c10-9-5-7-3-1-2-4-8(7)6-9/h1-4H,5-6H 
2,3-dihydro-1H-inden-2-one 
a-hydrindone 
|A-Hydrindone 
INDANONE 
C9H8O 
2-Indanone, 98% 5g 
C9-H8-O 
c0402 
CID11983 
2-methoxy-4-methyl-3-nitropyridine 
2-Indanone, 98% - 10G 10g 
EINECS 210-410-3 
C3303 
Literature

Title: Synthesis of indenoporphyrins, highly modified porphyrins with reduced diatropic characteristics.

Journal: The Journal of organic chemistry 20110701

Title: Calculation of the vibrationally resolved, circularly polarized luminescence of d-camphorquinone and (S,S)-trans-beta-hydrindanone.

Journal: Chemphyschem : a European journal of chemical physics and physical chemistry 20100802

Title: Diastereoisomers of 2-benzyl-2, 3-dihydro-2-(1H-inden-2-yl)-1H-inden-1-ol: potential anti-inflammatory agents.

Journal: Bioorganic & medicinal chemistry letters 20091015

Title: Bacterial degradation of aromatic compounds.

Journal: International journal of environmental research and public health 20090101

Title: Calorimetric and computational study of indanones.

Journal: The journal of physical chemistry. A 20071101

Title: Experimental study on the thermal oxidation of 2-chlorophenol in air over the temperature range 450-900 degrees C.

Journal: Chemosphere 20060301

Title: Aromatic and aliphatic hydrocarbon consumption and transformation by the styrene degrading strain Pseudomonas putida CA-3.

Journal: FEMS microbiology letters 20050815

Title: Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors.

Journal: Journal of medicinal chemistry 20050602

Title: Lipoprotein mutation accelerates substrate permeability-limited toluene dioxygenase-catalyzed reaction.

Journal: Biotechnology progress 20050101

Title: Syntheses of 2-substituted indoles and fused indoles by photostimulated reactions of o-iodoanilines with carbanions by the SRN1 mechanism.

Journal: The Journal of organic chemistry 20030404

Title: Synthesis of 2-indanones via [4 + 1] annulation reactions of (trialkylsilyl)arylketenes.

Journal: Organic letters 20020725

Title: New metabolites in the degradation of fluorene by Arthrobacter sp. strain F101.

Journal: Applied and environmental microbiology 19970301

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