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Bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indol]sulfat

bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indole] sulphate  Struktur
56396-94-2
CAS-Nr.
56396-94-2
Bezeichnung:
Bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indol]sulfat
Englisch Name:
bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indole] sulphate
Synonyma:
Cardian;Betagon;Mepicor;Corindolan;Corindocomb;Sulfate salt;MEPINDOLOL SULFATE;1-[(2-methyl-1H-indol-4-yl)oxy]-3-(propan-2-ylamino)propan-2-ol;bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indole] sulphate;Bis-[4-[2-hydroxy-3-(isopropylamino)-propoxy]-2-methyl-1H-indole]-sulfate
CBNumber:
CB1928318
Summenformel:
C30H46N4O8S
Molgewicht:
622.77324
MOL-Datei:
56396-94-2.mol

Bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indol]sulfat Eigenschaften

Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Bildanzeige (GHS) Skull and Crossbones (GHS06)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H301 Giftig bei Verschlucken. Akute Toxizit?t oral Kategorie 3 Achtung P264, P270, P301+P310, P321, P330,P405, P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P321 Besondere Behandlung
P330 Mund ausspülen.
P405 Unter Verschluss aufbewahren.
P501 Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indol]sulfat Chemische Eigenschaften,Einsatz,Produktion Methoden

Originator

Corindolan,Schering,W. Germany,1980

Manufacturing Process

The 4-hydroxy-2-methylindole (MP 112°C to 115°C from benzene/ethyl acetate), used as starting material, may be obtained by hydrogenation of 4- benzyloxy-2-dimethylamino-methylindole (MP 117°C to 120°C from benzene) in the presence of a palladium catalyst (5% on aluminum oxide).
11.6 g of 4-hydroxy-2-methylindole are added to a solution of 3.1 g of sodium hydroxide in 150 cc of water, and then 12.4 cc of epichlorhydrin are added while stirring and in an atmosphere of nitrogen. The reaction mixture is further stirred at room temperature for 24 hours, is extracted 4 times with methylene chloride, and the combined organic layers which have been dried over magnesium sulfate are concentrated by evaporation at reduced pressure. The resulting residue is taken up in 150 cc of dioxane and 50 cc of isopropylamine, and the mixture is heated to the boil for 6 hours. The reaction mixture is evaporated to dryness at reduced pressure, the residue is shaken 4 times between ethyl acetate and a 1 N aqueous tartaric acid solution, and a 5 N caustic soda solution is then added to the combined tartaric acid phases until an alkaline reaction is obtained. The alkaline solution is then shaken out 6 times with methylene chloride, the combined extracts are dried over magnesium sulfate, and the solvent is evaporated in a vacuum. The oily viscous residue may be crystallized from ethyl acetate. The title compound has a MP of 95°C to 97°C.

Therapeutic Function

Beta-adrenergic blocker

Bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indol]sulfat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indol]sulfat Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 2)Lieferanten
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56396-94-2(Bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indol]sulfat)Verwandte Suche:


  • bis[4-[2-hydroxy-3-(isopropylamino)propoxy]-2-methyl-1H-indole] sulphate
  • Bis-[4-[2-hydroxy-3-(isopropylamino)-propoxy]-2-methyl-1H-indole]-sulfate
  • MEPINDOLOL SULFATE
  • Betagon
  • Cardian
  • Corindocomb
  • Corindolan
  • Mepicor
  • Sulfate salt
  • 1-[(2-methyl-1H-indol-4-yl)oxy]-3-(propan-2-ylamino)propan-2-ol
  • 56396-94-2
  • C30H46N4O8S
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