2-Indanone
2-Indanone structure
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Common Name | 2-Indanone | ||
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| CAS Number | 615-13-4 | Molecular Weight | 132.159 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 248.9±29.0 °C at 760 mmHg | |
| Molecular Formula | C9H8O | Melting Point | 51-54 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 100.0±0.0 °C | |
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Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors.
J. Med. Chem. 48 , 3808-15, (2005) The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors an... |
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Synthesis of indenoporphyrins, highly modified porphyrins with reduced diatropic characteristics.
J. Org. Chem. 76(13) , 5335-45, (2011) Indene-fused porphyrins have been synthesized starting from 2-indanone. Knorr-type reaction of oximes derived from benzyl or tert-butyl acetoacetate with 2-indanone and zinc dust in propionic acid gave good yields of indenopyrroles. Treatment with N-chlorosuc... |
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Bromoform activation. TiCl4-Mg-promoted CHBr2- and CBr3- transfer to a variety of aldehydes and ketones.
Org. Lett. 15(22) , 5802-5, (2013) TiCl4-Mg can mediate addition of CHBr3 to a variety of aldehydes and ketones to form dibromomethyl carbinols and also be used to effect CBr3 transfer to carbonyl groups to form tribromomethyl carbinols. The successful application of TiCl4-Mg-promoted coupling... |
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Spectroscopic studies on photochemical formation of o-xylylene in solution. Fujiwara M, et al.
J. Phys. Chem. A 101(27) , 4912-15, (1997)
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