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| Nα-L-Valyl-N1-[1-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisoquinolin-1-yl)ethyl]glycinamide Basic information |
Product Name: | Nα-L-Valyl-N1-[1-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisoquinolin-1-yl)ethyl]glycinamide | Synonyms: | Amphibine I;Nα-L-Valyl-N1-[1-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisoquinolin-1-yl)ethyl]glycinamide;Glycinamide, L-valyl-N-[1-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl)ethyl]- | CAS: | 53098-67-2 | MF: | C21H34N4O4 | MW: | 406.52 | EINECS: | | Product Categories: | | Mol File: | 53098-67-2.mol | |
| Nα-L-Valyl-N1-[1-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisoquinolin-1-yl)ethyl]glycinamide Chemical Properties |
Boiling point | 628.0±55.0 °C(Predicted) | density | 1.120±0.06 g/cm3(Predicted) | pka | 13.80±0.46(Predicted) |
| Nα-L-Valyl-N1-[1-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisoquinolin-1-yl)ethyl]glycinamide Usage And Synthesis |
Description | A further alkaloid in the series of peptide bases obtained from Zizyphus amphibia
A. Cheval., this base is obtained as a pale yellow foam and has no definite melting
point. It is laevorotatory having a specific rotation of [α]20D - 50° (c 0.6, C6H6 ).
The ultraviolet spectrum in MeOH has a single absorption maximum at 282 nm. | References | Tschesche, Spilles, Eckhardt, Chern. Ber., 107, 1329 (1974) |
| Nα-L-Valyl-N1-[1-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisoquinolin-1-yl)ethyl]glycinamide Preparation Products And Raw materials |
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