423734
6-Methyl-1-indanone
99%
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About This Item
Empirical Formula (Hill Notation):
C10H10O
CAS Number:
Molecular Weight:
146.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
Product Name
6-Methyl-1-indanone, 99%
InChI
1S/C10H10O/c1-7-2-3-8-4-5-10(11)9(8)6-7/h2-3,6H,4-5H2,1H3
SMILES string
Cc1ccc2CCC(=O)c2c1
InChI key
DBOXRDYLMJMQBB-UHFFFAOYSA-N
assay
99%
form
solid
bp
70 °C/0.4 mmHg (lit.)
mp
60-62 °C (lit.)
functional group
ketone
Application
6-Methyl-1-indanone was used as a starting material for the synthesis of branched alkyl indanes (BINs).
General description
6-Methyl-1-indanone is a substituted indanone. It has been synthesized in high quantum yields by the photolysis of α-chloro-2′,5′-dimethylacetophenone. It is formed as one of the photoproduct during the irradiation of 2,5-dimethylphenacyl (DMP) esters. It is reported to be one of the semivolatile component of lamina cigarette smoke.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Comparisons of Smoke Components in the Semivolatile Phase from Lamina and Midrib Cigarettes of Flue-cured Tobacco Leaves.
Ishiguro S and Sugawara S.
Agricultural and Biological Chemistry, 42(8), 1527-1531 (1978)
2, 5-Dimethylphenacyl as a new photoreleasable protecting group for carboxylic acids.
Klan P, et al.
Organic Letters, 2(11), 1569-1571 (2000)
A laser flash photolysis study of the mechanism of the photocyclization of. alpha.-chloro-ortho-methylacetophenones.
Netto-Ferreira JC and Scaiano JC.
Journal of the American Chemical Society, 113(15), 5800-5803 (1991)
Rapid Photochemical Synthesis of 6-Methyl-1-Indanone.
Wang S, et al.
Advanced Materials Research, 634-638, 416-419 (2013)
Andrew M Booth et al.
Environmental science & technology, 42(21), 8122-8126 (2008-11-27)
Previously, comprehensive two-dimensional gas chromatography-time of flight-mass-spectrometry (GCxGC-ToF-MS) revealed that the unresolved complex mixtures (UCMs) of contaminant hydrocarbons accumulated by health-affected mussels Mytilus edulis (up to 125 microg g dry weight(-1)) collected from around U.K. coasts, included many isomeric branched
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