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| 1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONE Basic information |
| Product Name: | 1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONE | | Synonyms: | 4-Oxo-1,5,6,7-tetrahydroindole;1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONE;1,5,6,7-TETRAHYDRO-4H-INDOLE-4-ONE;1,5,6,7-TETRAHYDRO-INDOL-4-ONE;4-OXO-4,5,6,7-TETRAHYDROINDOLE;Tetrahydroindolone;4-0xo-4,5,6,7-tetrahydroindole;1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONE 97+% | | CAS: | 13754-86-4 | | MF: | C8H9NO | | MW: | 135.16 | | EINECS: | | Product Categories: | Building Blocks;C7 to C9;Heterocyclic Building Blocks;Indoles;Chemical Synthesis;Heterocyclic Building Blocks;Heterocyclic Compounds;Building Blocks | | Mol File: | 13754-86-4.mol |
| 1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONE Chemical Properties |
| Melting point | 188-190 °C (lit.) | | Boiling point | 311℃ | | density | 1.216 | | Fp | 150℃ | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | form | powder to crystal | | pka | 15.91±0.20(Predicted) | | color | White to Light yellow to Light orange | | CAS DataBase Reference | 13754-86-4(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-37/39 | | WGK Germany | 3 | | HS Code | 2914390090 |
| 1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONE Usage And Synthesis |
| Uses | • ;Reactant in synthesis of psammopemmin A as antitumor agent1• ;Reactant in synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoesters and tricyclic tetrahydrobenzindoles via C-H insertion reactions2• ;Reactant in preparation of tricyclic indole and dihydroindole derivatives as inhibitors of guanylate cyclase3• ;Reactant in preparation of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of (halobenzyl)pyrroles4• ;Reactant in enantioselective preparation of arylalkenyl indoles via asymmetric C-H insertion of rhodium carbenoids foll | | Uses | 1,5,6,7-Tetrahydro-4H-indol-4-one, is a versatile building block used for the synthesis of more complex pharmaceutical compounds. It can be used for the preparation of Psammopemmin A. | | General Description | Iodination of 1,5,6,7-tetrahydro-4H-indol-4-one using 1-chloromethyl--4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetra-fluoroborate) yields α-iodo derivative as the main product. |
| 1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONE Preparation Products And Raw materials |
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