Boiling point	87 ºC (13 mmHg)
Flash point	184 ºF
Density	1.035
Refractive index	1.453

Symbol(GHS)	Xn
Hazard Codes	R20;R37/38;R41
SDS/MSDS	S26;S39

Source	SDS/MSDS Samples
Alfa-Aesar	View & Download
Sigma-Aldrich	View & Download

Synthetic Route

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Articles

Peer-Reviewed Papers

Synthesis and biological evaluation of achiral indole-substituted titanocene dichloride derivatives.Anthony Deally et al.International journal of medicinal chemistry, 2012, 905981-905981 (2012-01-01) Engineering Styrene Monooxygenase for Biocatalysis: Reductase-Epoxidase Fusion Proteins.Thomas Heine et al.Applied biochemistry and biotechnology, 181(4), 1590-1610 (2016-11-11) Total synthesis of (+/-)-perophoramidine.James R Fuchs et al.Journal of the American Chemical Society, 126(16), 5068-5069 (2004-04-22) A facile synthesis of Tyrian purple based on a biosynthetic pathway. Tanoue Y, et al. Fisheries Science (Tokyo, Japan), 67(4), 726-729 (2001) Indoline derivatives as 5-HT(2C) receptor agonists.J M Bentley et al.Bioorganic & medicinal chemistry letters, 14(9), 2367-2370 (2004-04-15) Synthesis of N-protected Nortopsentins B and D. Moody CJ and Roffey JRA. ARKIVOC (Gainesville, FL, United States), 1, 393-401 (2000) Efficient synthesis of 5-and 6-tributylstannylindoles and their reactivity with acid chlorides in the Stille coupling reaction. Cherry K, et al. Tetrahedron Letters, 48(33), 5751-5753 (2007) Enantioselective total syntheses of (+)-arborescidine A, (-)-arborescidine B, and (-)-arborescidine C.Leonardo S Santos et al.The Journal of organic chemistry, 69(4), 1283-1289 (2004-02-14) Palladium-catalyzed carbonylation of haloindoles: No need for protecting groups. Kumar K, et al. Organic Letters, 6(1), 7-10 (2004)

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