| Name | α-Methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanamine Monohydrochloride |
|---|---|
| Synonyms |
1-[5-(2-Thienylmethoxy)-1H-indol-3-yl]propan-2-amine hydrochloride (1:1)
A-Methyl-5-(2-Thienylmethox BW 723C8 BW723C86HCl a-Methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanamine Monohydrochloride 1-(5-(Thiophen-2-ylmethoxy)-1H-indol-3-yl)propan-2-amine hydrochloride BW 723C86 hydrochlor α-methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanaminehydrochloride BW 723C86[B175] ALPHA-METHYL-5-(2-THIENYLMETHOXY)-1H-INDOLE-3-ETHANAMINE HYDROCHLORIDE BW-723C86 (BW 723C86 Α-METHYL-5-(2-THIENYLMETHOXY)-1H-INDOLE-3-,ETHANAMINEMONOHYDROCHLORIDE(BW723C86) BW 723C86 BW 723C86 HYDROCHLORIDE Zinc02379519 a-methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanaminehydrochloride 1-[5-(thiophen-2-ylmethoxy)-1H-indol-3-yl]propan-2-amine,hydrochloride ALPHA-METHYL-5-(2-THIENYLMETHOXY)-1H-INDOLE-3-ETHANAMINE, MONOHYDROCHLORIDE BW 723C86 \ 5-HT2B SEROTONIN RECTOR AG ONIST 1-[5-(2-Thienylmethoxy)-1H-indol-3-yl]-2-propanamine hydrochloride (1:1) 1H-Indole-3-ethanamine, α-methyl-5-(2-thienylmethoxy)-, hydrochloride (1:1) MFCD01321066 |
| Description | BW-723C86 is a potent and a selective 5-HT2B receptor agonist. BW-723C86 exhibits anxiolytic-like actions. BW-723C86 also causes hyperphagia and reduced grooming in rats[1][2][3]. |
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| Related Catalog | |
| Target |
5-HT2B Receptor |
| References |
| Boiling Point | 488.4ºC at 760 mmHg |
|---|---|
| Melting Point | 203 - 205 °C |
| Molecular Formula | C16H19ClN2OS |
| Molecular Weight | 322.853 |
| Flash Point | 249.2ºC |
| Exact Mass | 322.090668 |
| PSA | 79.28000 |
| LogP | 5.20040 |
| Vapour Pressure | 1.09E-09mmHg at 25°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| RTECS | NL8504715 |
| HS Code | 2934999090 |
| HS Code | 2934999090 |
|---|---|
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |