3-(2-Aminoethyl)-5-fluoro-1H-indole
5-Fluorotryptamine
CAS: 576-16-9
Molecular Formula: C10H11FN2
3-(2-Aminoethyl)-5-fluoro-1H-indole - Names and Identifiers
| Name | 5-Fluorotryptamine |
| Synonyms | AKOS B030092 5-FLUOROTRYPTAMINE 5-Fluorotryptamine RARECHEM AN KA 1417 1H-Indole-3-ethanamine, 5-fluoro- 3-(2-AMINOETHYL)-5-FLUORO-1H-INDOLE 3-(2-Aminoethyl)-5-fluoro-1H-indole 2-(5-Fluoro-1H-indol-3-yl)ethylamine 2-(5-FLUORO-1H-INDOL-3-YL)-ETHYLAMINE 3-(2-Aminoethyl)-5-fluoro-1H-indole hydrochloride 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl dihydrogen phosphate |
| CAS | 576-16-9 |
| InChI | InChI=1/C10H6F17O4P/c11-3(12,1-2-31-32(28,29)30)4(13,14)5(15,16)6(17,18)7(19,20)8(21,22)9(23,24)10(25,26)27/h1-2H2,(H2,28,29,30) |
3-(2-Aminoethyl)-5-fluoro-1H-indole - Physico-chemical Properties
| Molecular Formula | C10H11FN2 |
| Molar Mass | 178.21 |
| Density | 1.249±0.06 g/cm3(Predicted) |
| Melting Point | 273-275 °C |
| Boling Point | 346.0±27.0 °C(Predicted) |
| Flash Point | 137.786°C |
| Vapor Presure | 0mmHg at 25°C |
| pKa | 16.37±0.30(Predicted) |
| Storage Condition | Room Temprature |
| Refractive Index | 1.324 |
3-(2-Aminoethyl)-5-fluoro-1H-indole - Risk and Safety
| Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. R22 - Harmful if swallowed |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
3-(2-Aminoethyl)-5-fluoro-1H-indole - Reference Information
| application | 5-fluorotryptamine can be used as an intermediate in pharmaceutical synthesis. |
| preparation | the preparation of 5-fluorotryptamine is as follows: indole and POCl3 react at normal temperature in DMF solvent to obtain compound 2. Compound 2 is dissolved in nitromethane and catalyzed by ammonium acetate to generate compound 3. Using anhydrous tetrahydrofuran as a solvent, dissolve compound 3 into it, add tetrahydrolithium aluminum, and react under anhydrous conditions to obtain compound 45-fluoryptamine. |
Last Update：2024-04-10 22:29:15
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