Detail of "36215-07-3"

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Preparation and electrochemical properties of N,N-disubstituted 1-amino-3-(9-anthryl)propane derivatives

Preparation and electrochemical properties of N,N-disubstituted 1-amino-3-(9-anthryl)propane derivatives. Hamann, H. J.; Pragst, F.; Jugelt, W. 36215-07-3 are also occured in this study. (Sekt. Chem., Humboldt-Univ., Berlin, E.Some commonly used reagents like 36215-07-3 is used in this experiment. Ger.). J. Prakt. Chem., 318(3), 369-80 (German) 1976. CODEN: JPCEAO. DOCUMENT TYPE: Journal CA Section: 26 (Condensed Aromatic Compounds) Section cross-reference(s): 72 The title compds. I (R1 = Me, R2 = H, Me, MeO, Ph, R3 = H, R2 = MeO, Ph, R3 = Me, Ph; R1 = Et, R2 = R3 = H; R1 = 4-MeOC6H4, R2 = MeO, R3 = H) and II (R4 = phenothiazin-9-yl, phenoxazin-9-yl, carbazol-9-yl) were prepd. in 6.5-43% yields by reaction of the amines R1NHC6H4R2-4, phenothiazine, phenoxazine, or carbazole K salt with the corresponding bromides II. III (R3 = H, Ph, Me) were prepd. in 9-17% yield by Grignard reaction of anthrone, phenylanthrone, or PhCHMeC6H4CN-2, resp., with MeO(CH2)3Cl. Anodic oxidn. of I or II in MeCN gave cation radicals IV (R1s as above) or V (X = S, O, bond line), whereas cathodic redn. gave anion radicals VI. No interaction between the amine and the anthracene parts of the mols. could be detected in the case of the radical ions. ..

Preparation and electrochemical properties of N,N-disubstituted 1-amino-3-(9-anthryl)propane derivatives

Preparation and electrochemical properties of N,N-disubstituted 1-amino-3-(9-anthryl)propane derivatives. Hamann, H. J.; Pragst, F.; Jugelt, W. 36215-07-3 are also occured in this study. (Sekt. Chem., Humboldt-Univ., Berlin, E.Some commonly used reagents like 36215-07-3 is used in this experiment. Ger.). J. Prakt. Chem., 318(3), 369-80 (German) 1976. CODEN: JPCEAO. DOCUMENT TYPE: Journal CA Section: 26 (Condensed Aromatic Compounds) Section cross-reference(s): 72 The title compds. I (R1 = Me, R2 = H, Me, MeO, Ph, R3 = H, R2 = MeO, Ph, R3 = Me, Ph; R1 = Et, R2 = R3 = H; R1 = 4-MeOC6H4, R2 = MeO, R3 = H) and II (R4 = phenothiazin-9-yl, phenoxazin-9-yl, carbazol-9-yl) were prepd. in 6.5-43% yields by reaction of the amines R1NHC6H4R2-4, phenothiazine, phenoxazine, or carbazole K salt with the corresponding bromides II. III (R3 = H, Ph, Me) were prepd. in 9-17% yield by Grignard reaction of anthrone, phenylanthrone, or PhCHMeC6H4CN-2, resp., with MeO(CH2)3Cl. Anodic oxidn. of I or II in MeCN gave cation radicals IV (R1s as above) or V (X = S, O, bond line), whereas cathodic redn. gave anion radicals VI. No interaction between the amine and the anthracene parts of the mols. could be detected in the case of the radical ions. ..