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| | 2-(3,4-Dihydro-2H-quinolin-1-yl)-ethylamine Basic information | | Uses |
| Product Name: | 2-(3,4-Dihydro-2H-quinolin-1-yl)-ethylamine | | Synonyms: | CHEMBRDG-BB 4003435;N-(2-Aminoethyl)-1,2,3,4-tetrahydroquinoline;2-(3,4-Dihydroquinolin-1(2H)-yl)ethanamine;1(2H)-Quinolineethanamine, 3,4-dihydro-;2-(3,4-dihydroquinolin-1(2H)-yl)ethanamine(SALTDATA: 2HCl 0.2H2O);2-(3,4-dihydro-2H-quinolin-1-yl)ethanamine;N-(β-aminoethyl)tetrahydroquinoline;2-[3,4-Dihydroquinolin-1(2H)-yl]ethylamine | | CAS: | 37481-18-8 | | MF: | C11H16N2 | | MW: | 176.26 | | EINECS: | | | Product Categories: | | | Mol File: | 37481-18-8.mol |  |
| | 2-(3,4-Dihydro-2H-quinolin-1-yl)-ethylamine Chemical Properties |
| Boiling point | 130-132 °C(Press: 5 Torr) | | density | 1.0645 g/cm3 | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | pka | 8.80±0.10(Predicted) |
| | 2-(3,4-Dihydro-2H-quinolin-1-yl)-ethylamine Usage And Synthesis |
| Uses | N-(2-Aminoethyl)-1,2,3,4-Tetrahydroquinoline is an organic intermediate that has been reported in the literature as a potential candidate for preparing PARP-1 inhibitors. | | Synthesis | 2-(3,4-Dihydro-2H-quinolin-1-yl)-ethylamine can be obtained by nucleophilic substitution of 1,2,3,4-tetrahydroquinoline and 2-bromoethylamine hydrobromide. |
| | 2-(3,4-Dihydro-2H-quinolin-1-yl)-ethylamine Preparation Products And Raw materials |
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