Skip to main content

  | मौसम…

411 समाचार
Public archive edition · Attributed source reporting with original dates · AI drafts are excluded

411 REFERENCE · Wikipedia

2,6-Dichloro-4-nitroaniline

Reference material by Wikipedia contributors. This retains its source identity and is not 411 news reporting.

Dichloran.svg 110 2,6-Dichloro-4-nitroaniline Amino-2,6-dichloro-4-nitrobenzene; Dicloran; Allisan; Batran; Bortran; Botran; Ditranil; Resisan 99-30-9 correct CAS 202-746-4 27864 504381 7152 C11000 7430 F0BE9UC5J7 1S/C6H4Cl2N2O2/c7-4-1-3(10(11)12)2-5(8)6(4)9/h1-2H,9H2 BIXZHMJUSMUDOQ-UHFFFAOYSA-N C1=C(C=C(C(=C1Cl)N)Cl)[N+](=O)[O-] 6 4 2 2 2 yellow solid10.1039/J19710002181 Crystal structure of 2,6-dichloro-4-nitroaniline 1971 Hughes David L. Trotter James Journal of the Chemical Society A: Inorganic, Physical, Theoretical 2181 1.624 g/cm3 191 130 2 torr 6.3 mg/l 2,6-Dichloro-4-nitroaniline https://pubchem.ncbi.nlm.nih.gov/compound/7430#section=Safety-and-Hazards pubchem.ncbi.nlm.nih.gov en 06 08 09 Danger 300 310 330 373 411 260 262 264 270 271 273 280 284 301+316 302+352 304+340 316 319 320 321 330 361+364 391 403+233 405 501 2,6-Dichloro-4-nitroaniline is an organic compound with the formula O2NC6H2Cl2NH2. It is the most widely discussed isomer of dichloronitroaniline, mainly as a precursor to the azo dye disperse brown 1. It is prepared by treatment of 4-nitroaniline with a mixture of hydrochloric acid and hydrogen peroxide (a source of chlorine). Gerald Booth vanc Nitro Compounds, Aromatic Ullmann's Encyclopedia of Industrial Chemistry 2007 Wiley-VCH Weinheim 978-3-527-30385-4 10.1002/14356007.a17_411 6th10.1002/14356007.o03_o08 Azo Dyes, 4. Cationic Dyes Ullmann's Encyclopedia of Industrial Chemistry 2011 Raue Roderich Kunde Klaus Engel Aloys 978-3-527-30385-4 References Category:Anilines