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RAC 8-HYDROXY EFAVIRENZ

RAC 8-HYDROXY EFAVIRENZ Struktur
205754-33-2
CAS-Nr.
205754-33-2
Englisch Name:
RAC 8-HYDROXY EFAVIRENZ
Synonyma:
8-HydroxyEfavirenz;RAC 8-HYDROXY EFAVIRENZ;8-hydroxy Efavirenz (Standard);8-Hydroxyefavirenz/205754-33-2;Efavirenz Impurity 11(8-Hydroxy Efavirenz);(4S)-6-chloro-4-(2-cyclopropylethynyl)-8-hydroxy-4-(trifluoromethyl)-1H-3,1-benzoxazin-2-one;6-Chloro-4-(cyclopropyl-d4-ethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one;2H-3,1-Benzoxazin-2-one,6-chloro-4-(cyclopropylethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-, (4S)-;(S)-6-Chloro-4-(cyclopropylethynyl)-8-hydroxy-4-(trifluoromethyl)-1,4-dihydro-2H-benzo[d][1,3]oxazin-2-one;2H-3,1-Benzoxazin-2-one, 6-chloro-4-(2-cyclopropylethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-, (4S)-
CBNumber:
CB7501021
Summenformel:
C14H9ClF3NO3
Molgewicht:
331.67
MOL-Datei:
205754-33-2.mol

RAC 8-HYDROXY EFAVIRENZ Eigenschaften

Schmelzpunkt:
144-154°C
Siedepunkt:
373.6±42.0 °C(Predicted)
Dichte
1+-.0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
L?slichkeit
Acetonitrile: soluble; DMSO: soluble; Methanol: soluble
Aggregatzustand
A solid
pka
7.18±0.40(Predicted)
Farbe
White to off-white
InChI
InChI=1S/C14H9ClF3NO3/c15-8-5-9-11(10(20)6-8)19-12(21)22-13(9,14(16,17)18)4-3-7-1-2-7/h5-7,20H,1-2H2,(H,19,21)/t13-/m0/s1
InChIKey
OOVOMPCQLMFEDT-ZDUSSCGKSA-N
SMILES
N1C2=C(O)C=C(Cl)C=C2[C@@](C#CC2CC2)(C(F)(F)F)OC1=O

Sicherheit

RAC 8-HYDROXY EFAVIRENZ Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

8-hydroxy Efavirenz is a major oxidative metabolite of the non-nucleoside reverse transcriptase inhibitor efavirenz . 8-hydroxy Efavirenz is formed when efavirenz is metabolized by the cytochrome P450 (CYP) isoform CYP2B6. It induces apoptosis in rat primary hippocampal neurons and loss of dendritic spines in rat primary hippocampal neuronal cultures when used at a concentration of 0.01 μM.

Chemische Eigenschaften

Off-White Solid

Verwenden

A labellebed metabolite of Efavirenz, a nonnucleoside HIV-1 reverse transcriptase inhibitor

RAC 8-HYDROXY EFAVIRENZ Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


RAC 8-HYDROXY EFAVIRENZ Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 45)Lieferanten
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Standardpharm Co. Ltd.
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BOC Sciences 16314854226
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Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627
info@efebio.com China 9804 58
Shanghai Hongye Biotechnology Co. Ltd 400-9205774
sales@glpbio.cn China 6777 58
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 +86-13028896684;
sales@rrkchem.com China 57422 58

  • RAC 8-HYDROXY EFAVIRENZ
  • 8-HydroxyEfavirenz
  • 6-Chloro-4-(cyclopropyl-d4-ethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one
  • (4S)-6-chloro-4-(2-cyclopropylethynyl)-8-hydroxy-4-(trifluoromethyl)-1H-3,1-benzoxazin-2-one
  • Efavirenz Impurity 11(8-Hydroxy Efavirenz)
  • 2H-3,1-Benzoxazin-2-one, 6-chloro-4-(2-cyclopropylethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-, (4S)-
  • 8-Hydroxy EfavirenzQ: What is 8-Hydroxy Efavirenz Q: What is the CAS Number of 8-Hydroxy Efavirenz Q: What is the storage condition of 8-Hydroxy Efavirenz Q: What are the applications of 8-Hydroxy Efavirenz
  • 2H-3,1-Benzoxazin-2-one,6-chloro-4-(cyclopropylethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-, (4S)-
  • (S)-6-Chloro-4-(cyclopropylethynyl)-8-hydroxy-4-(trifluoromethyl)-1,4-dihydro-2H-benzo[d][1,3]oxazin-2-one
  • 8-Hydroxyefavirenz/205754-33-2
  • 8-hydroxy Efavirenz (Standard)
  • 205754-33-2
  • Metabolites
  • Non-nucleoside Reverse Transcriptase
  • Pharmaceuticals
  • Intermediates & Fine Chemicals
  • Isotope Labeled Compounds
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