Legality of Cannabis by U.S. Jurisdiction

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Description Ball-and-stick model of the (S) enantiomer of VX. Systematic name generated in ChemDraw: (S)-S-2-(diisopropylamino)ethyl O-ethyl methylphosphonothioate. Image based on structural data from this 3DChem.com model.[dead link] Cf. John H, Balszuweit F, Kehe K, Worek F & Thiermann H (2015) "Toxicokinetic Aspects of Nerve Agents and Vesicants" in Gupta, Ramesh C. , ed. Handbook of Toxicology of Chemical Warfare Agents (2nd ed.), Cambridge, MA: Academic Press, pp. 817−856, esp. 823 [Fig.56.1] ISBN: 0128004940. . The crystal structures of closely related molecules have been reported: V. G. Andrianov et al., Zh. Strukt. Khim. (1981) 22, 68-1 (MEPVAL) and A. M. Sorensen, Acta. Cryst. B (1977) 33, 2693 (IPEMPI).
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current21:19, 17 March 2008Thumbnail for version as of 21:19, 17 March 20081,100 × 706 (155 KB)Benjah-bmm27{{Information |Description = Ball-and-stick model of the (''S'') enantiomer of VX. Systematic name generated in ChemDraw: (''S'')-''S''-2-(diisopropylamino)ethyl ''O''-ethyl methylphosphonothioate. Image based on structural data from [http://www.3dchem.co
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