4-ACETYL-1-(CHLOROMETHYL)-6-HYDROXY-1,2,3,4-TETRAHYDROBENZO-[F]-QUINOLINE
Compound with spectra: 1 NMR
![4-ACETYL-1-(CHLOROMETHYL)-6-HYDROXY-1,2,3,4-TETRAHYDROBENZO-[F]-QUINOLINE](/api/compound/1Zh9NkUbnl6.png?ph=true&h=300&w=458 "4-ACETYL-1-(CHLOROMETHYL)-6-HYDROXY-1,2,3,4-TETRAHYDROBENZO-[F]-QUINOLINE")
| SpectraBase Compound ID | 1Zh9NkUbnl6 |
|---|---|
| InChI | InChI=1S/C16H16ClNO2/c1-10(19)18-7-6-11(9-17)16-13-5-3-2-4-12(13)15(20)8-14(16)18/h2-5,8,11,20H,6-7,9H2,1H3/t11-/m1/s1 |
| InChIKey | JXWRNCLBMVWQIF-LLVKDONJSA-N |
| Mol Weight | 289.76 g/mol |
| Molecular Formula | C16H16ClNO2 |
| Exact Mass | 289.086956 g/mol |
| Enantiomer InChIKey | JXWRNCLBMVWQIF-NSHDSACASA-N |
| Racemate InChIKey | JXWRNCLBMVWQIF-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
7,8-Dihydro-6H-thieno[3,2-e]indole-2,6-dicarboxylic acid, 6-(2,2,2-trichloroethyl) 2-ethyl ester
rel-(1S,3R,4S)-3,4-dihydro-4-hydroxy-6-methoxy-1,3-dimethylnaphtho[1,2-c]pyran
benzo[h]quinolin-2(1H)-one, 4-(2-chloro-6-fluorophenyl)-3,4-dihydro-
1-(3-BROMO-4-HYDROXY-5-METHOXYPHENYL)-3-OXO-1,2,3,4-TETRAHYDROBENZO-[F]-QUINOLINE
1,1'-Binaphthalene, 1,2-dihydro-2',3-dimethoxy-
1-(3-chloro-4-hydroxy-5-methoxyphenyl)-1,4-dihydrobenzo[f]quinolin-3(2H)-one
1-[2-[cyclohexyl(methyl)amino]-1-naphthalenyl]-2-naphthalenol
4-[1,4-Dihydro-2,6-dimethyl-3,5-di(ethoxycarbonyl)pyridin-4-yl]-2,2,5,5-tetramethyl-tetrahydropyrrol-1-yloxy radical
1(2H)-quinolineethanol, 6-[2-[2-chloro-4-(methylsulfonyl)phenyl]diazenyl]-3,4-dihydro-2,2,4,7-tetramethyl-, acetate (ester)
1-(chloroacetyl)-4-(4-chlorophenyl)-2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline
| Title | Journal or Book | Year |
|---|---|---|
| Design, Synthesis, and Evaluation of CC-1065 and Duocarmycin Analogs Incorporating the 2,3,10,10a-Tetrahydro-1H-cyclopropa[d]benzo[f]quinol-5-one (CBQ) Alkylation Subunit: Identification and Structural Origin of Subtle Stereoelectronic Features That Govern Reactivity and Regioselectivity | Journal of the American Chemical Society | 1994 |