2,4,6-Tribromoaniline

Chemical compound 2,4,6-Tribromoaniline.svg 120px Skeletal formula skin-invert 2,4,6-tribromoaniline space-filling model.png The space-filling model of 2,4,6-tribromoaniline bg-transparent 2,4,6-Tribromoaniline ball-and-stick.png The ball and stick model of 2,4,6-tribromoaniline bg-transparent 2,4,6-Tribromoaniline 147-82-0 8986 205-700-1 0C2N8WIL3B 21106171 C1=C(C=C(C(=C1Br)N)Br)Br 1S/C6H4Br3N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2 GVPODVKBTHCGFU-UHFFFAOYSA-N 6 4 3 1 120 300 Insoluble Harmful, Corrosive, Toxic 05 06 07 08 Danger 301 302 311 312 315 318 319 331 332 373 260 261 264 270 271 280 301+310 301+312 302+352 304+312 304+340 305+351+338 310 311 312 314 321 322 330 332+313 337+313 361 362 363 403+233 405 501 2 0 0 Non-flammable Non-flammable 2,4,6-Tribromoaniline is a brominated derivative of aniline with the formula C6H4Br3N. It is used in organic synthesis of pharmaceuticals, agrochemicals and fire-extinguishing agents.https://labmonk.com/synthesis-of-2-4-6-tribromoaniline-from-aniline Synthesis of 2,4,6-tribromoaniline from aniline Synthesis 2,4,6-Tribromoaniline can be prepared by treating bromine water with aniline in a solution of acetic acid or dilute hydrochloric acid: none|thumb|309x309px|By reacting bromine with aniline in water, a white precipitate (2,4,6-tribromoaniline) immediately forms. Reactions Diazotization, then reaction with ethanol to replace the diazonium group with hydrogen, gives 1,3,5-tribromobenzene.Organic Syntheses sym.-Tribromobenzene Coleman G. H. Talbot William F. 1933 13 96 10.15227/orgsyn.013.0096 free See also Bromine test 4-Bromoaniline 2,4,6-Tribromoanisole 2,4,6-Tribromophenol References Category:Anilines Category:Bromoarenes