1,5,6,7-Tetrahydro-4H-indol-4-one
1,5,6,7-Tetrahydro-4H-indol-4-one structure
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Common Name | 1,5,6,7-Tetrahydro-4H-indol-4-one | ||
|---|---|---|---|---|
| CAS Number | 13754-86-4 | Molecular Weight | 135.163 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 310.6±11.0 °C at 760 mmHg | |
| Molecular Formula | C8H9NO | Melting Point | 188-190 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 149.6±26.7 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Direct α-iodination of aryl alkyl ketones by elemental iodine activated by 1-chloromethyl-4-fluoro-1, 4-diazoniabicyclo [2.2. 2] octane bis (tetrafluoroborate). Jereb M, et al.
Synthesis 06 , 0853-0858, (2003)
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DNA binders: 1. evaluation of DNA-interactive ability, design, and synthesis of novel intercalating agents Sechi M, et al.
Lett. Drug Des. Discov. 6(1) , 56-62, (2009)
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Synthesis of pyrrolo [1, 2-a] indole-1, 8 (5H)-diones as new synthons for developing novel tricyclic compounds of pharmaceutical interest. Sechi M, et al.
ARKIVOC 5 , 97-106, (2004)
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Synthesis of (R)-and (S)-1-formyl-6, 7, 8, 9-tetrahydro-N, N-(dipropyl)-3H-benz [e] indol-8-amines: potent and orally active 5-HT1A receptor agonists. Lin C-H, et al.
J. Heterocycl. Chem. 31(1) , 129-39, (1994)
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