I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
It is used in organic synthesis, wittig reagent.
Meenakshisundaram Kalyanasundari; Krishnaswamy Panchanatheswaran; Ward T. Robinson; Huo Wen. Reactions of benzoylmethylenetriphenylphosphorane with mercury(II) halides: spectral and structural characterization of [(C6H5)3PCHCOC6H5 · HgCl2]2 · 2CH3OH and [(C6H5)3PCHCOC6H5 · HgI2]2. Journal of Organometallic Chemistry. 1995, 491 (1-2), 103-109.
M. Mohan Raj; A. Dharmaraja; K. Panchanatheswaran; K.A. Venkatesan; T.G. Srinivasan; P.R. Vasudeva Rao. Extraction of fission palladium(II) from nitric acid by benzoylmethylenetriphenylphosphorane (BMTPP). Analytica Chimica Acta. 2006, 84 (1-2), 118-124.
Stable ylide which reacts with aldehydes to give ɑß-unsaturated ketones. See Appendix 1. For preparation of unsubstituted vinyl ketones from this and related ylides with paraformaldehyde, see: Synthesis, 31 (1970).
Can be converted by C-acylation to a diacylphosphorane, which can be oxidized to a 1,2,3-triketone. For reaction scheme, see N,O-Bis(trimethylsilyl)acetamide, L00183.
Gefahrenhinweise (EU): H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.