1,4-Benzodioxin-5-carboxamide, 8-amino-7-chloro-N-[(2S)-1,4-diazabicyclo[2.2.2]oct-2-ylmethyl]-2,3-dihydro-
1,4-Benzodioxin-5-carboxamide, 8-amino-7-chloro-N-[(2S)-1,4-diazabicyclo[2.2.2]oct-2-ylmethyl]-2,3-dihydro- Basic information
- Product Name:
- 1,4-Benzodioxin-5-carboxamide, 8-amino-7-chloro-N-[(2S)-1,4-diazabicyclo[2.2.2]oct-2-ylmethyl]-2,3-dihydro-
- Synonyms:
-
- 5-HT3-In-1
- 1,4-Benzodioxin-5-carboxamide, 8-amino-7-chloro-N-[(2S)-1,4-diazabicyclo[2.2.2]oct-2-ylmethyl]-2,3-dihydro-
- 5HT3In1,5 HT3 In 1,5-HT-3-In-1
- CAS:
- 186348-68-5
- MF:
- C16H21ClN4O3
- MW:
- 352.82
- Mol File:
- 186348-68-5.mol
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1,4-Benzodioxin-5-carboxamide, 8-amino-7-chloro-N-[(2S)-1,4-diazabicyclo[2.2.2]oct-2-ylmethyl]-2,3-dihydro- Chemical Properties
- Boiling point:
- 482.3±45.0 °C(Predicted)
- Density
- 1.46±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Soluble in DMSO
- pka
- 13.27±0.20(Predicted)
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1,4-Benzodioxin-5-carboxamide, 8-amino-7-chloro-N-[(2S)-1,4-diazabicyclo[2.2.2]oct-2-ylmethyl]-2,3-dihydro- Usage And Synthesis
Uses
5-HT3-In-1 is extracted from patent EP0748807A1, compound example 8. It shows 5-HT3 inhibition activity.
IC 50
5-HT3 Receptor
References
[1] Jegham S, et al. Derivatives of N-(1,4-diazabicyclo(2.2.2)-oct-2-yl)methyl benzamide, their preparation and their therapeutical use. EP0748807A1.
1,4-Benzodioxin-5-carboxamide, 8-amino-7-chloro-N-[(2S)-1,4-diazabicyclo[2.2.2]oct-2-ylmethyl]-2,3-dihydro-Supplier
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