| Name | 4-hydroxy-5-undecyl-1,3-benzothiazole-6,7-dione |
|---|---|
| Synonyms |
3-UNDECYL-2-HYDROXYDIOXOBENZOTHIAZOL
6-HYDROXY-5-UNDECYL-1,3-BENZOTHIAZOLE-4,7-DIONE UHDBT 4,7-Benzothiazoledione,6-hydroxy-5-undecyl 6-hydroxy-5-undecyl-4,7-benzothiazoledione 6-hydroxy-5-undecyl-benzothiazole-4,7-dione |
| Description | UHDBT is a cytochrome bc1 complex Qo site inhibitor. UHDBT can be used for electron transfer research[1]. |
|---|---|
| Related Catalog | |
| Target |
Qo[1]. |
| References |
| Density | 1.179g/cm3 |
|---|---|
| Boiling Point | 489.8ºC at 760 mmHg |
| Molecular Formula | C18H25NO3S |
| Molecular Weight | 335.46 |
| Flash Point | 250ºC |
| Exact Mass | 335.15600 |
| PSA | 95.50000 |
| LogP | 5.09850 |
| Index of Refraction | 1.56 |
|
~%
43152-58-5 |
| Literature: Friedman,M.D. et al. Journal of Medicinal Chemistry, 1973 , vol. 16, p. 1314 - 1316 |
| Precursor 2 | |
|---|---|
| DownStream 0 | |