![]() 3-Methylindanone structure
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Common Name | 3-Methylindanone | ||
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CAS Number | 6072-57-7 | Molecular Weight | 146.186 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 226.7±10.0 °C at 760 mmHg | |
Molecular Formula | C10H10O | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 87.5±14.0 °C |
Theory and use of the pseudophase model in gas-liquid chromatographic enantiomeric separations.
Anal. Chem. 78(1) , 113-9, (2006) The theory and use of the "three-phase" model in enantioselective gas-liquid chromatography utilizing a methylated cyclodextrin/polysiloxane stationary phase is presented for the first time. Equations are derived that account for all three partition equilibri... |
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Unresolved complex mixtures (UCMs) of aromatic hydrocarbons: branched alkyl indanes and branched alkyl tetralins are present in UCMs and accumulated by and toxic to, the mussel Mytilus edulis.
Environ. Sci. Technol. 42(21) , 8122-6, (2008) 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 micr... |
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Synthesis of chiral 3-alkyl-3,4-dihydroisocoumarins by dynamic kinetic resolutions catalyzed by a Baeyer-Villiger monooxygenase.
J. Org. Chem. 75(6) , 2073-2076, (2010) Baeyer-Villiger monooxygenases have been tested in the oxidation of racemic benzofused ketones. When employing a single mutant of phenylacetone monooxygenase (M446G PAMO) under the proper reaction conditions, it was possible to achieve 3-substituted 3,4-dihyd... |
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New Friedel-Crafts Chemistry. XVI. 1 A Reconsideration of Cyclialkylation and Competing Reactions of Certain Phenylalkyl, Benzoylalkyl and Acetylphenylalkyl Chlorides. Khalaf AA and Roberts RM.
J. Org. Chem. 31(1) , 89-95, (1966)
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Photochemical bromination of substituted indan-1-one derivatives: synthesis of new polybromoindan-1-one derivatives. KUS, NS.
Turk. J. Chem. 33(4) , 479-486, (2009)
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Electrophilic substitution at saturated carbon. XLIII. Alkylammonium carbanide ion-pair reorganization reactions in base-catalyzed 1,3-proton transfer in an indene system. Almy J and Cram DJ.
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Asymmetric induction during transfer of triplet energy. Ouannes C, et al.
J. Am. Chem. Soc. 95(25) , 8472-8474, (1973)
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Thiocarbonyls. VI. Studies in the Indanone and Tetralone Series1. Campaigne E and Moss RD.
J. Am. Chem. Soc. 76(5) , 1269-1271, (1954)
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Microwave-assisted one-pot synthesis of 1-indanones from arenes and alpha,beta-unsaturated acyl chlorides.
J. Org. Chem. 71(11) , 4312-4315, (2006) A series of 1-indanones were synthesized in good yields via tandem Friedel-Crafts acylation and Nazarov cyclization of arenes and alpha,beta-unsaturated acyl chlorides in the presence of aluminum chloride under microwave irradiation. |
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Photochemistry of ketones in solution--49. A study of photosensitized splitting of dimethylthymine dimers.
Photochem. Photobiol. 25(3) , 239-242, (1977)
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