2-Methoxy-4-nitroaniline

2-Methoxy-4-nitroaniline.svg 110px 2-Methoxy-4-nitroaniline 4-Nitro-o-anisidine, 4-Nitroanisidine 97-52-9 1518220 7060 202-588-6 7337 DPU26P1846 1S/C7H8N2O3/c1-12-7-4-5(9(10)11)2-3-6(7)8/h2-4H,8H2,1H3 GVBHRNIWBGTNQA-UHFFFAOYSA-N COC1=C(C=CC(=C1)[N+](=O)[O-])N 7 8 3 2 yellow solid 1.42 g/cm310.1107/S0108270191010739 Structure of 2-methoxy-4-nitroaniline 1992 Mehdi S. Acta Crystallographica Section C Crystal Structure Communications 48 4 749–751 1992AcCrC..48..749M 140–142 07 08 09 Warning 302 351 411 203 261 264 264+265 270 271 273 280 301+317 302+352 304+340 305+351+338 318 319 321 330 332+317 337+317 362+364 391 403+233 405 501 2-Methoxy-4-nitroaniline is an organic compound with the formula O2NC6H3(OCH3)NH2.10.1021/acs.jced.9b00991 2-Methoxy-4-nitroaniline Solubility in Several Monosolvents: Measurement, Correlation, and Solvent Effect Analysis 2020 Bao Yuxin Wu Jiaxin Zhao Xi Zhao Hongkun Journal of Chemical & Engineering Data 65 2 757–765 It is one of four isomers of methoxynitroaniline. The compound is a precursor to the commercial Pigment Yellow 74. Safety It induces expression of some versions of cytochrome P450.10.1016/S0304-4165(97)00118-9 2-Methoxy-4-nitroaniline and its isomers induce cytochrome P4501A (CYP1A) enzymes with different selectivities in the rat liver 1998 Degawa Masakuni Nakayama Masafumi Konno Yoshihiro Masubuchi Kazuhiro Yamazoe Yasushi Biochimica et Biophysica Acta (BBA) - General Subjects 1379 3 391–398 9545601 References Category:Anilines Category:Nitrobenzene derivatives Category:Methoxy compounds