CAS 146887-38-9
:2(3H)-Furanone,5-(4-chlorophenyl)dihydro-3-phenyl-3-(1H-1,2,4-triazol-1-ylmethyl)-,(3R,5R)-rel-
Description:
2(3H)-Furanone, 5-(4-chlorophenyl)dihydro-3-phenyl-3-(1H-1,2,4-triazol-1-ylmethyl)-, (3R,5R)-rel- is a chemical compound characterized by its complex structure, which includes a furanone ring, a chlorophenyl group, and a triazole moiety. This compound is notable for its potential biological activity, often explored in pharmaceutical research for its antimicrobial or antifungal properties. The presence of the triazole ring is significant, as triazoles are known for their ability to inhibit certain enzymes and are commonly used in the development of antifungal agents. The stereochemistry indicated by (3R,5R)- suggests specific spatial arrangements of atoms that can influence the compound's reactivity and interaction with biological targets. Additionally, the chlorophenyl group may enhance lipophilicity, affecting the compound's solubility and permeability. Overall, this compound exemplifies the intricate relationship between molecular structure and biological function, making it a subject of interest in medicinal chemistry.
Formula:C19H16ClN3O2
Synonyms:- 2(3H)-Furanone,5-(4-chlorophenyl)dihydro-3-phenyl-3-(1H-1,2,4-triazol-1-ylmethyl)-, cis-
- Rh9129
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Found 4 products.
Fenbuconazole-lactone B R-9130
CAS:Controlled ProductFormula:C19H16ClN3O2Color and Shape:NeatMolecular weight:353.80Fenbuconazole-lactone B rh-9130
CAS:Fenbuconazole-lactone B rh-9130 is an azole fungicide, which is a chemically synthesized compound. It is derived from the lactone form of fenbuconazole, an established triazole fungicide, and designed to inhibit sterol biosynthesis. Its mode of action involves disrupting the synthesis of ergosterol, a critical component of fungal cell membranes, thereby impeding fungal growth and reproduction.Formula:C19H16ClN3O2Purity:Min. 95%Molecular weight:353.8 g/mol
