2,6-Dichloropyridine

C5H3Cl2N.svg 122px 2,6-Dichloropyridine 2402-78-0 correct FDA WM26PC2SBW 3561947 16095 219-282-3 16989 1S/C5H3Cl2N/c6-4-2-1-3-5(7)8-4/h1-3H FILKGCRCWDMBKA-UHFFFAOYSA-N C1=CC(=NC(=C1)Cl)Cl 5 3 2 1 white solid 1.665 g/cm310.1002/chem.202303643 The Impact of ortho -substituents on Bonding in Silver(I) and Halogen(I) Complexes of 2-Mono- and 2,6-Disubstituted Pyridines: An In-Depth Experimental and Theoretical Study 2024 Kumar Parveen Rautiainen J. Mikko Novotný Jan Ward Jas S. Marek Radek Rissanen Kari Puttreddy Rakesh Chemistry – A European Journal 30 13 e202303643 38055221 free 86-89 211-212 06 07 Danger 301 315 319 335 261 264 270 271 280 301+310 302+352 304+340 305+351+338 312 321 330 332+313 337+313 362 403+233 405 501 2,6-Dichloropyridine is a chloropyridine with the formula C5H3Cl2N. A white solid, it is one of six isomers of dichloropyridine. It serves as a precursor to the antibiotic enoxacin,Shinkichi Shimizu Nanao Watanabe Toshiaki Kataoka Takayuki Shoji Nobuyuki Abe Sinji Morishita Hisao Ichimura Pyridine and Pyridine Derivatives 2007 10.1002/14356007.a22_399 as well as the drug anpirtoline and the antifungal liranaftate. Synthesis 2,6-Dichoropyridine is produced by reaction of pyridine with chlorine. 2-Chloropyridine is an intermediate. Toxicity The is 115 mg/kg (oral, mice). References Category:Chloropyridines Category:Disubstituted pyridines