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It is used as pharmaceutical intermediates. It is used in the synthesis of indole phytoalexin cyclobrassinon. And also in unprecedented chemical structure and biomimetic synthesis of erucalexin, a phytoalexin from the wild crucifer Erucastrum gallicum.
H. D. Hollis Showalter.; Anthony D. Sercel.; Boguslawa M. Leja.; Craig D. Wolfangel.; Linda A. Ambroso.; William L. Elliott.; David W. Fry .; Alan J. Kraker.; Curtis T. Howard.; Gina H. Lu.; Charles W. Moore.; James M. Nelson.; Bill J. Roberts.; Patrick W. Vincent.; William A. Denny.; Andrew M. Thompson. Tyrosine Kinase Inhibitors. 6. Structure-Activity Relationships among N- and 3-Substituted 2,2-Diselenobis(1H-indoles) for Inhibition of Protein Tyrosine Kinases and Comparative in Vitro and in Vivo Studies against Selected Sulfur Congeners.J. Med. Chem. 1997, 40 (4),413-426.
Justin R. Harrison.; Christopher J. Moody. The Horner-Wadsworth-Emmons reaction in the synthesis of macrocyclic peptides: the Trp-His-Gly-Arg derived macrocycle of moroidin. Tetrahedron Lett. 2003, 44 (28),5189-5191.
Gefahrenhinweise (EU): H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves. 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.