2,3-Dichloroaniline

2,3-Dichloranilin.svg 2,3-Dichloroaniline 1-amino-2,3-dichlorobenzene 608-27-5 46636 1889723 21111810 210-157-9 601687 11844 2BL4F1DXVN 3442 1590 1S/C6H5Cl2N/c7-4-2-1-3-5(9)6(4)8/h1-3H,9H2 BRPSAOUFIJSKOT-UHFFFAOYSA-N C1=CC(=C(C(=C1)Cl)Cl)N 2 6 5 1 colorless oil 1.383 g/cm3 24 252 2.78 1.5969 2,3-Dichloroaniline https://pubchem.ncbi.nlm.nih.gov/compound/11844#section=GHS-Classification pubchem.ncbi.nlm.nih.gov en 06 07 08 09 Danger 301 311 315 317 331 373 410 260 261 262 264 270 271 272 273 280 301+316 302+352 304+340 316 319 321 330 332+317 333+317 361+364 362+364 391 403+233 405 501 2,3-Dichloroaniline is an organic compound with the formula C6H3Cl2(NH2). It is one of several isomers of dichloroaniline. It is a colorless oil although commercial samples often appear colored. It is produced by hydrogenation of 2,3-dichloronitrobenzene.P. F. Vogt J. J. Gerulis Amines, Aromatic Ullmann’s Encyclopedia of Industrial Chemistry 2005 Wiley-VCH Weinheim 10.1002/14356007.a02_037 9783527303854 Safety and environmental aspects Its 72-h EC50 is 6.75 mg/L. 10.1016/j.chemosphere.2011.05.023 Toxicity of 58 substituted anilines and phenols to algae Pseudokirchneriella subcapitata and bacteria Vibrio fischeri: Comparison with published data and QSARs 2011 Aruoja Villem Sihtmäe Mariliis Dubourguier Henri-Charles Kahru Anne Chemosphere 84 10 1310–1320 21664645 2011Chmsp..84.1310A Biodegradation of 2,3-dichloroaniline proceeds via initial ring hydroxylation.10.1021/acs.est.4c02173 Compound-Specific Carbon, Nitrogen, and Hydrogen Isotope Analysis to Characterize Aerobic Biodegradation of 2,3-Dichloroaniline by a Mixed Enrichment Culture 2024 Suchana Shamsunnahar Araujo Sofia Pimentel Lomheim Line Mack E. Erin Spain Jim C. Edwards Elizabeth Passeport Elodie Environmental Science & Technology 58 27 12042–12050 38934904 2024EnST...5812042S References Category:Anilines Category:Dichlorophenyl compounds