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Product Details
23593-75-1 Name |
|
Name |
Clotrimazole |
Synonym |
myclo;(2-Chlorophenyl)diphenyl-1-imidazolylmethane;(Chlorotrityl)imidazole;1-((2-chlorophenyl)diphenylmethyl)-1h-imidazol;1-(alpha-(2-Chlorophenyl)benzhydryl)imidazole;1-(o-chloro-alpha,alpha-diphenylbenzyl)-imidazol;1-[(2-chlorophenyl)diphenylmethyl]-1h-imidazol;1-(o-Chloro-α,α-diphenylbenzyl)imidazole |
23593-75-1 Chemical & Physical Properties |
|
Melting point |
147-149ºC |
Boiling point |
482.3±40.0 °C at 760 mmHg |
Density |
1.1±0.1 g/cm3 |
Molecular Formula |
C22H17ClN2 |
Molecular Weight |
344.837 |
Flash Point |
245.5±27.3 °C |
PSA |
17.82000 |
LogP |
5.44 |
Exact Mass |
344.108032 |
Vapour Pressure |
0.0±1.2 mmHg at 25°C |
Index of Refraction |
1.617 |
Storage condition |
Store at RT. |
Water Solubility |
Soluble in chloroform, DMSO, DMF and alcohols |
23593-75-1 Description |
Clotrimazole is an imidazole derivative, an antifungal compound and is a CYP (cytochrome P450) inhibitor.Target: Antifungal; CYPClotrimazole (brand name Canesten or Lotrimin) is an antifungal medication commonly used in the treatment of fungal infections (of both humans and other animals) such as vaginal yeast infections, oral thrush, and ringworm. It is also used to treat athlete's foot and jock itch.It is commonly available as an over-the-counter substance in various dosage forms, such as a cream, and also (especially in the case of ear infection) as a combination medicine. It is also available as a troche or throat lozenge (prescription only). For ear infection, it is often applied in liquid form, as ear drops.The antimycotic drug clotrimazole inhibits the function of the gastric H,K-ATPase in a manner similar to that observed for the Na,K-ATPase. Because of the high hydrophobicity of the compound, the interaction between clotrimazole and the ion pump occurs at the membrane domain in the apolar core of the membrane. The enzymatic activity was inhibited with a half-saturating concentration of 5.2 microM. Various partial reactions of the pump cycle were analyzed with the electrochromic styryl dye RH421 that has been widely used to study the transport mechanism of P-type ATPases. |
23593-75-1 Uses |
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This article reports an efficient synthesis of triarylmethanes and tetraarylmethanes from chlorohydrocarbons with miscellaneous nucleophiles in fluorinated alcohols, featuring metal-free, wide substrate scope, excellent functional group tolerance, and mild reaction conditions.
The invention discloses a synthesis method of clotrimazole, and belongs to the technical field of chemical synthesis. According to the method, 2-chlorotrityl chloride and imidazole are taken as raw materials, hexafluoroisopropanol is taken as a solvent, and reaction is performed in an alkali environment.
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