I2002
1,3-Indandione
97%
Synonym(s):
1,3-Dioxoindan
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About This Item
Empirical Formula (Hill Notation):
C9H6O2
CAS Number:
Molecular Weight:
146.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-109-7
Beilstein/REAXYS Number:
1210061
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
129-132 °C (lit.)
SMILES string
O=C1CC(=O)c2ccccc12
InChI
1S/C9H6O2/c10-8-5-9(11)7-4-2-1-3-6(7)8/h1-4H,5H2
InChI key
UHKAJLSKXBADFT-UHFFFAOYSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Abdolmajid Bayandori Moghaddam et al.
Chemical & pharmaceutical bulletin, 54(10), 1391-1396 (2006-10-04)
This is an environmentally friendly method in the field of electroorganic reactions under controlled potential electrolysis, without toxic reagents at a carbon electrode in an undivided cell which involves the (EC) mechanism reaction and comprises two steps alternatively; (i) electrochemical
A Schulman et al.
Journal of the American Veterinary Medical Association, 188(4), 402-405 (1986-02-15)
Five cases of coagulopathy caused by consumption of indanedione (diphacinone)-based rodenticides are reported. In each case, acute onset of lethargy and respiratory distress were the predominant initial clinical signs. Thoracic radiography revealed pulmonary edema, pleural effusion, and/or pericardial effusion as
V Violet Dhayabaran et al.
Luminescence : the journal of biological and chemical luminescence, 32(7), 1339-1348 (2017-05-19)
A novel Schiff base, (S,Z)-4-(methylthio)-2-((3-oxo-2,3-dihydro-1H-inden-1-ylidene)amino)butanoic acid (L) and four M(II) complexes (where M = Co, Cu, Ni and Zn) were synthesized and characterized. The DNA-binding characteristics of the complexes were investigated using various spectroscopic methods and viscosity measurements. Analysis of the results
Bilquees Bano et al.
Bioorganic chemistry, 81, 658-671 (2018-09-27)
Current study deals with the evaluation of indane-1,3-dione based compounds as new class of urease inhibitors. For that purpose, benzylidine indane-1,3-diones (1-30) were synthesized and fully characterized by different spectroscopic techniques including EI-MS, HREI-MS, 1H, and 13C NMR. All synthetic
A R Murthy et al.
Journal of medicinal chemistry, 28(11), 1591-1596 (1985-11-01)
A series of 2-substituted indan-1,3-dione derivatives, including alkyl (C-1-C-5), mono- and disubstituted phenyl, and other 2-aryl derivatives, were tested for hypolipidemic activity of CF1 male mice at 20 mg/kg per day. These derivatives reduced both serum cholesterol and triglycerides after
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