Introduction:Basic information about Buparvaquone CAS 88426-33-9, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Buparvaquone Basic information
| Product Name: | Buparvaquone |
| Synonyms: | CS-1178;2-((4-(1,1-dimethylethyl)cyclohexyl)methyl)-3-hydroxy-4-naphthalenedione;2-((4-tert-butylcyclohexyl)methyl)-3-hydroxy-1,4-naphthoquinone;butalex;2-[[4-(1,1-dimethylethyl)cyclohexyl]methyl]-3-hydroxy-1,4-naphthalenedione;BW-720C;2-((4-tert-butylcyclohexyl)Methyl)-3-hydroxynaphthalene-1,4-dione;Buparvaquone-d4 |
| CAS: | 88426-33-9 |
| MF: | C21H26O3 |
| MW: | 326.43 |
| EINECS: | 618-162-1 |
| Product Categories: | API;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;john's |
| Mol File: | 88426-33-9.mol |
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Buparvaquone Chemical Properties
| Melting point | 178-184°C |
| Boiling point | 460.7±45.0 °C(Predicted) |
| density | 1.158±0.06 g/cm3(Predicted) |
| storage temp. | Sealed in dry,2-8°C |
| solubility | DMSO: soluble |
| pka | 5.04±0.10(Predicted) |
| form | powder |
| color | Yellow |
| Major Application | forensics and toxicology veterinary |
| InChI | InChI=1S/C21H26O3/c1-21(2,3)14-10-8-13(9-11-14)12-17-18(22)15-6-4-5-7-16(15)19(23)20(17)24/h4-7,13-14,24H,8-12H2,1-3H3 |
| InChIKey | KLLIVCPQDTYMLC-UHFFFAOYSA-N |
| SMILES | C1(=O)C2=C(C=CC=C2)C(=O)C(O)=C1CC1CCC(C(C)(C)C)CC1 |
| CAS DataBase Reference | 88426-33-9(CAS DataBase Reference) |
Safety Information
| WGK Germany | 3 |
| RTECS | QJ5766600 |
| Storage Class | 11 - Combustible Solids |
| Toxicity | LD50 orally in rats: >2 g/kg (Hudson) |
Buparvaquone Usage And Synthesis
| Chemical Properties | Yellow Crystalline Solid |
| Uses | Analog of antimalarial hydroxynaphthoquinones; tert-butyl derivative of Parvaquone. Antiprotozoal (Theileria) |
| Biological Activity | Buparvaquone is a second-generation hydroxynaphthoquinone antiprotozoal drug related to parvaquone and atovaquone. Buparvaquone is indicated for the therapy and prophylaxis of all forms of Theileriosis and found to have an anti-Leishmanial activity. |
| in vivo | Treatment of N.?caninum infected mice with buparvaquone (100?mg/kg) either by intraperitoneal injection or gavage prevents neosporosis symptoms in 4 out of 6 mice in the intraperitoneally treated group, and in 6 out of 7 mice in the group receiving oral treatment[1]. Both a hydrous gel and water-in-oil emulsion of buparvaquone significantly reduce cutaneous parasite burden and lesion size, compared with the untreated control[3]. |
Buparvaquone Preparation Products And Raw materials