2-Methyltetrahydroquinoline

2-Methyltetrahydroquinoline.png 2-Methyl-1,2,3,4-tetrahydroquinoline Tetrahydroquinaldine, 1,2,3,4-Tetrahydroquinaldine 1780-19-4 racemic (R/S) 63430-95-5 (R) 200125-70-8 (S) 86920 1151452 1151451 correct FDA XHV42AW48X 96289 1376640 1376639 217-226-2 277-887-8 DTXSID80928096 589607 1S/C10H13N/c1-8-6-7-9-4-2-3-5-10(9)11-8/h2-5,8,11H,6-7H2,1H3/t8-/m1/s1 JZICUKPOZUKZLL-MRVPVSSYSA-N 1S/C10H13N/c1-8-6-7-9-4-2-3-5-10(9)11-8/h2-5,8,11H,6-7H2,1H3/t8-/m0/s1 JZICUKPOZUKZLL-QMMMGPOBSA-N CC1CCC2=CC=CC=C2N1 C[C@@H]1CCC2=CC=CC=C2N1 C[C@H]1CCC2=CC=CC=C2N1 10 13 1 colorless oil 125 (17 Torr) 07 Warning 315 319 264 280 302+352 305+351+338 321 332+313 337+313 362 2-Methyltetrahydroquinoline is one of the methyl-substituted derivatives of tetrahydroquinoline. A colorless oil, it is a chiral compound owing to the presence of the methyl substituent. It is produced by the hydrogenation of quinaldine.10.1021/ja504523b 24877556 A Molecular Iron Catalyst for the Acceptorless Dehydrogenation and Hydrogenation of N-Heterocycles 2014 Chakraborty Sumit Brennessel William W. Jones William D. Journal of the American Chemical Society 136 24 8564–8567 2014JAChS.136.8564C It is of interest in medicinal chemistry.10.1021/cr100307m 21830756 Advances in the Chemistry of Tetrahydroquinolines 2011 Sridharan Vellaisamy Suryavanshi Padmakar A. Menéndez J. Carlos Chemical Reviews 111 11 7157–7259 References Category:Tetrahydroquinolines