(2R,3R)-Methyl 7-Fluoro-2-(4-Fluorophenyl)-3-(1-Methyl-1H-1,2,4-Triazol-5-Yl)-4-Oxo-1,2,3,4-Tetrahydroquinoline-5-Carboxylate

98%

Reagent Code: #231734
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CAS Number 1425767-92-5

science Other reagents with same CAS 1425767-92-5

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Weight 398.36 g/mol
Formula C₂₀H₁₆F₂N₄O₃
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Used in the synthesis of antifungal pharmaceuticals, particularly as an intermediate in the production of triazole-based drugs. Its structure supports activity against a range of pathogenic fungi by inhibiting essential enzyme functions in fungal cell membranes. Commonly employed in research and development for novel antifungal agents due to its fluorinated aromatic and heterocyclic components, which enhance bioavailability and binding affinity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize antifungal potency and reduce toxicity.

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inventory 100mg
10-20 days ฿39,000.00

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(2R,3R)-Methyl 7-Fluoro-2-(4-Fluorophenyl)-3-(1-Methyl-1H-1,2,4-Triazol-5-Yl)-4-Oxo-1,2,3,4-Tetrahydroquinoline-5-Carboxylate
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Used in the synthesis of antifungal pharmaceuticals, particularly as an intermediate in the production of triazole-based drugs. Its structure supports activity against a range of pathogenic fungi by inhibiting essential enzyme functions in fungal cell membranes. Commonly employed in research and development for novel antifungal agents due to its fluorinated aromatic and heterocyclic components, which enhance bioavailability and binding affinity. Also utilized in medicinal chemistry for structure-activity

Used in the synthesis of antifungal pharmaceuticals, particularly as an intermediate in the production of triazole-based drugs. Its structure supports activity against a range of pathogenic fungi by inhibiting essential enzyme functions in fungal cell membranes. Commonly employed in research and development for novel antifungal agents due to its fluorinated aromatic and heterocyclic components, which enhance bioavailability and binding affinity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize antifungal potency and reduce toxicity.

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