2-Indolinethione

Indolidine-2-thione.svg 180px 1,3-Dihydro-2H-indole-2-thione 1,3-Dihydroindole-2-thione 496-30-0 correct CAS correct FDA S9SC88MKF6 tautomer 53497-58-8 1345979 2297319 11341121 692-228-8 3032310 Q4596893 1S/C8H7NS/c10-8-5-6-3-1-2-4-7(6)9-8/h1-4H,5H2,(H,9,10) IGJWTYFTQNHSEK-UHFFFAOYSA-N C1C2=CC=CC=C2NC1=S 8 7 1 1 white solid 1.27 g/cm3 44-45 2-Indolinethione https://pubchem.ncbi.nlm.nih.gov/compound/3032310#section=Safety-and-Hazards pubchem.ncbi.nlm.nih.gov en 07 Warning 302 315 319 335 261 264 264+265 270 271 280 301+317 302+352 304+340 305+351+338 317 319 321 330 332+317 337+317 362+364 403+233 405 501 2-Indolinethione is an organic compound with the formula C8H6(S)(NH). It is a derivative of dihydroindole containing a thione group. The compound is a tautomer of 2-mercaptoindole. A white solid, it is prepared by thiation of 2-oxindole.10.1248/cpb.17.550 Thiation of Oxindoles 1969 Hino Tohru Tsuneoka Kazuko Nakagawa Masako Akaboshi Sanya Chemical and Pharmaceutical Bulletin 17 3 550–558 free 10.1021/jo101865y Thionations Using a P4S10−Pyridine Complex in Solvents Such as Acetonitrile and Dimethyl Sulfone 2011 Bergman Jan Pettersson Birgitta Hasimbegovic Vedran Svensson Per H. The Journal of Organic Chemistry 76 6 1546–1553 21341727 2-Indolinethione is a precursor to several natural products.10.1021/jo0479866 Concise Syntheses of the Cruciferous Phytoalexins Brassilexin, Sinalexin, Wasalexins, and Analogues: Expanding the Scope of the Vilsmeier Formylation 2005 Pedras M. Soledade C. Jha Mukund The Journal of Organic Chemistry 70 5 1828–1834 15730307 References Category:Indolines Category:Thioamides