Androst-4-en-3,11,17-trion Produkt Beschreibung

Adrenosterone Struktur
382-45-6
  • CAS-Nr.382-45-6
  • Bezeichnung:Androst-4-en-3,11,17-trion
  • Englisch Name:Adrenosterone
  • Synonyma:Androst-4-en-3,11,17-trion
    Nsc12166;s substance G;ADRENOSTERONE;Andrenosterone;Reichstein'REICHSTEIN'S 'G';REICHSTEIN'S ''G'';11-Oxo/Adrenosterone;11-KETOANDROSTENEDIONE;REICHSTEIN'S SUBSTANCE G
  • CBNumber:CB1765508
  • Summenformel:C19H24O3
  • Molgewicht:300.39
  • MOL-Datei:382-45-6.mol
Androst-4-en-3,11,17-trion physikalisch-chemischer Eigenschaften
  • Schmelzpunkt: :219-222 °C(lit.)
  • alpha  :300 º (c=1 in chloroform)
  • Siedepunkt: :381.62°C (rough estimate)
  • Dichte :1.1381 (rough estimate)
  • Brechungsindex :290 ° (C=0.2, EtOH)
  • storage temp.  :Refrigerator
  • Optische Aktivität :[α]20/D +300°, c = 1 in chloroform
  • Merck  :14,176
  • InChIKey :RZRPTBIGEANTGU-IRIMSJTPSA-N
  • CAS Datenbank :382-45-6(CAS DataBase Reference)
  • NIST chemische Informationen :Androst-4-ene-3,11,17-trione(382-45-6)
Sicherheit
  • WGK Germany  :3

Adrenosterone Chemische Eigenschaften,Einsatz,Produktion Methoden

  • Chemische Eigenschaften Off-White to Pale Yellow Solid
  • Verwenden Androgenic activity;Androgenic steroid
  • Verwenden Steroid hormone with weak androgenic effects.
  • läuterung methode Dissolve adrenosterone i n Me2CO, decolorise it with charcoal, filter, add H2O, Me2CO evaporate and the solid is recrystallised from aqueous EtOH. Also recrystallise it from Et2O or Et2O/pentane and dry it at 110o/0.1mm for 2hours. It can be sublimed under high vacuum. [Reichstein Helv Chim Acta 20 953, 979 1937, Mason et al. J Biol Chem 116 267 1936, Beilstein 7 III 4601.]
Adrenosterone Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Androst-4-en-3,11,17-trion Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
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382-45-6, Adrenosterone Verwandte Suche:
  • Nsc12166
  • 11-Keto-4-androstene-3,17-dione
  • 11-Oxo-4-androstene-3,17-dione
  • 4-Androstene-3,11,17-trione Reichstein's Substance G
  • Reichstein&apos
  • s substance G
  • (8S,9S,10R,13S,14S)-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11,17-trione
  • 11-Oxo/Adrenosterone
  • REICHSTEIN'S SUBSTANCE G
  • REICHSTEIN'S SUBSTANCE 'G'
  • REICHSTEIN'S ''G''
  • REICHSTEIN'S 'G'
  • Adrenosterone ((+)-Adrenosterone)
  • 11-KETOANDROSTENEDIONE
  • 4-ANDROSTENE-3,11,17-TRIONE
  • 4-ANDROSTEN-3,11,17-TRIONE
  • ANDROST-4-ENE-3,11,17-TRIONE
  • ADRENOSTERONE
  • 11-Oxy-4-androstenedione
  • Adrenosterone;Androst-4-ene-3,11,17-trione;Reichstein's substance G
  • 11-Ketoandrostenedione, 4-Androstene-3,11,17-trione, Androst-4-ene-3,11,17-trione, Reichsteins substance G
  • (8β,9α,10β,14α,13β)-Androsta-4-ene-3,11,17-trione
  • Andrenosterone
  • 382-45-6
  • 328-45-6
  • Complex Molecules
  • Chiral Building Blocks
  • Asymmetric Synthesis
  • Steroids
  • 17-Ketosteroids
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