| Identification | Back Directory | [Name]
RAC 8-HYDROXY EFAVIRENZ | [CAS]
205754-33-2 | [Synonyms]
8-HydroxyEfavirenz
RAC 8-HYDROXY EFAVIRENZ
6-Chloro-4-(cyclopropyl-d4-ethynyl)-1,4-dihydro-8-hydroxy-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one | [Molecular Formula]
C14H5D4ClF3NO3 | [MDL Number]
MFCD09840726 | [MOL File]
205754-33-2.mol | [Molecular Weight]
331.67 |
| Chemical Properties | Back Directory | [Appearance]
Off-White Solid | [Melting point ]
144-154°C | [Boiling point ]
373.6±42.0 °C(Predicted) | [density ]
1?+-.0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
Acetonitrile: soluble; DMSO: soluble; Methanol: soluble | [form ]
A solid | [pka]
7.18±0.40(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White Solid | [Uses]
8-Hydroxy Efavirenz is a metabolite of Efavirenz (E425000), a nonnucleoside HIV-1 reverse transcriptase inhibitor. | [Uses]
A labellebed metabolite of Efavirenz, a nonnucleoside HIV-1 reverse transcriptase inhibitor | [Description]
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. |
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| Company Name: |
BOC Sciences
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16314854226 |
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www.bocsci.com |
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DC Chemicals
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021-58447131 13564518121 |
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https://www.chemicalbook.com/ShowSupplierProductsList927327/0.htm |
| Company Name: |
Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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