N-(2,4-difluorophenyl)-4,4-dimethyl-3-oxopentanamide

≥97%

Reagent Code: #220438
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CAS Number 497059-96-8

science Other reagents with same CAS 497059-96-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.26 g/mol
Formula C₁₃H₁₅F₂NO₂
badge Registry Numbers
MDL Number MFCD01567378
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of antifungal agents, particularly in the development of triazole-based pharmaceuticals. Its structure supports metabolic stability and enhances lipophilicity, which improves tissue penetration and bioavailability in active drug compounds. Commonly employed in research for novel dermatological treatments targeting fungal infections. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize antifungal potency and reduce toxicity.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿7,380.00

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N-(2,4-difluorophenyl)-4,4-dimethyl-3-oxopentanamide
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Used as an intermediate in the synthesis of antifungal agents, particularly in the development of triazole-based pharmaceuticals. Its structure supports metabolic stability and enhances lipophilicity, which improves tissue penetration and bioavailability in active drug compounds. Commonly employed in research for novel dermatological treatments targeting fungal infections. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize antifungal potency and reduce toxi

Used as an intermediate in the synthesis of antifungal agents, particularly in the development of triazole-based pharmaceuticals. Its structure supports metabolic stability and enhances lipophilicity, which improves tissue penetration and bioavailability in active drug compounds. Commonly employed in research for novel dermatological treatments targeting fungal infections. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize antifungal potency and reduce toxicity.

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