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| 4,5,6,7-TETRAHYDROINDOLE Basic information |
| Product Name: | 4,5,6,7-TETRAHYDROINDOLE | | Synonyms: | 4,5,6,7-TETRAHYDROINDOLE;4,5,6,7-TETRAHYDRO-1H-INDOLE;4,5,6,7-TETRAHYDROINDOLE 98+%;1H-Indole, 4,5,6,7-tetrahydro-;2,3-Tetramethylenepyrrole;Cyclohex[b]pyrrole;NSC 122455;4,5,6,7-Tetrahydroindole 98% | | CAS: | 13618-91-2 | | MF: | C8H11N | | MW: | 121.18 | | EINECS: | | Product Categories: | Building Blocks;Heterocyclic Building Blocks;Indoles | | Mol File: | 13618-91-2.mol |
| 4,5,6,7-TETRAHYDROINDOLE Chemical Properties |
| Melting point | 53-57 °C(lit.) | | storage temp. | 2-8°C | | BRN | 108853 | | InChIKey | KQBVVLOYXDVATK-UHFFFAOYSA-N |
| 4,5,6,7-TETRAHYDROINDOLE Usage And Synthesis |
| Uses | 4,5,6,7-Tetrahydro-1H-indole is used in preparation of chiral tetraaryl-substituted Methane. Also, used in preparation of 4-substituted Phenylamidine derivatives used for controlling phytopathogenic microorganisms. | | Uses | 4,5,6,7-Tetrahydroindole was used as reactant in:- synthesis of ethyl 3-(4,5,6,7-tetrahydroindol-2-yl)-2-propynoate
- preparation of BODIPY dyes
- N-alkylation with chloromethyloxirane
- preparation of hydroindolepropynoate by chemo- and regioselective solvent-free ethynylation
- palladium- and copper-free cross-coupling of halopropynoates
- preparation of carbonylalkenyl indoles via coupling with dicarbonyl compounds
- 1:2 annelation of 4,5,6,7-tetrahydroindole with 1-benzoyl-2-phenylacetylene
| | General Description | 4,5,6,7-Tetrahydroindoles, due to their easy aromatization, are good intermediates to synthesize indoles. 4,5,6,7-Tetrahydroindole on condensation with cyanoacetate leads to 1-ethylthio-2-cyano-4,5,6,7-tetrahydrocyclohexa-[c]-3H-pyrrolizin-3-one. |
| 4,5,6,7-TETRAHYDROINDOLE Preparation Products And Raw materials |
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