Identification | Back Directory | [Name]
cis-Atovaquone | [CAS]
137732-39-9 | [Synonyms]
cis-Atovaquone cis-Atovaquone-d4 Atovaquone EP Imp B Atovaquone Impurity 17 Atovaquone EP Impurity B Atovaquone EP Impurity B (RC A) Atovaquone Impurity 2(Atovaquone EP Impurity B) Atovaquone EP Impurity B (Atovaquone Related Compound A) Atovaquone EP Impurity B (Atovaquone USP Related Compound A) 2-[cis-4-(4-Chlorophenyl)cyclohexyl]-3-hydroxynaphthalene-1,4-dione 1,4-Naphthalenedione,2-[cis-4-(4-chlorophenyl)cyclohexyl]-3- hydroxy- 2-((1s,4s)-4-(4-chlorophenyl)cyclohexyl)-3-
hydroxynaphthalene-1,4-dione | [Molecular Formula]
C22H19ClO3 | [MDL Number]
MFCD28137497 | [MOL File]
137732-39-9.mol | [Molecular Weight]
366.84 |
Chemical Properties | Back Directory | [Melting point ]
>40°C (dec.) | [Boiling point ]
535.0±50.0 °C(Predicted) | [density ]
1.349±0.06 g/cm3(Predicted) | [storage temp. ]
Room Temperature, under inert atmosphere | [solubility ]
Chloroform (Slightly), Dichloromethane (Slightly, Acetonitrile) | [form ]
Solid | [pka]
5.01±0.10(Predicted) | [color ]
Pale Yellow to Light Yellow |
Hazard Information | Back Directory | [Uses]
cis-Atovaquone is the cis-isomer of Atovaquone (A793500), a hydroxynaphthoquinone derivative that inhibits mitochondrial electron transport. | [Definition]
ChEBI: Atovaquone is a naphthoquinone compound having a 4-(4-chlorophenyl)cyclohexyl group at the 2-position and a hydroxy substituent at the 3-position. It has a role as an antimalarial, an antifungal agent, an EC 1.3.5.2 [dihydroorotate dehydrogenase (quinone)] inhibitor, an EC 1.6.5.3 [NADH:ubiquinone reductase (H(+)-translocating)] inhibitor and an EC 1.10.2.2 (quinol--cytochrome-c reductase) inhibitor. It is a member of monochlorobenzenes and a hydroxy-1,4-naphthoquinone. |
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Company Name: |
BOC Sciences
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Website: |
www.bocsci.com |
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