[2-fluoro-4-[2-(4-methoxyphenyl)ethynyl]phenyl]-[(3R)-3-hydroxypiperidin-1-yl]methanone

≥98%(HPLC)

Reagent Code: #204043
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CAS Number 1443118-44-2

science Other reagents with same CAS 1443118-44-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 353.39 g/mol
Formula C₂₁H₂₀FNO₃
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used in the pharmaceutical industry as an intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It plays a role in the development of targeted cancer therapies due to its structural features that enable selective binding to specific enzyme sites. The compound's fluorinated aromatic system and chiral hydroxypiperidine moiety contribute to enhanced metabolic stability and improved receptor affinity. Commonly employed in research settings for structure-activity relationship (SAR) studies aimed at optimizing drug candidates for improved potency and pharmacokinetic profiles.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿18,120.00
inventory 25mg
10-20 days ฿56,640.00

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[2-fluoro-4-[2-(4-methoxyphenyl)ethynyl]phenyl]-[(3R)-3-hydroxypiperidin-1-yl]methanone
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Used in the pharmaceutical industry as an intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It plays a role in the development of targeted cancer therapies due to its structural features that enable selective binding to specific enzyme sites. The compound's fluorinated aromatic system and chiral hydroxypiperidine moiety contribute to enhanced metabolic stability and improved receptor affinity. Commonly employed in research settings for structure-activity rela

Used in the pharmaceutical industry as an intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It plays a role in the development of targeted cancer therapies due to its structural features that enable selective binding to specific enzyme sites. The compound's fluorinated aromatic system and chiral hydroxypiperidine moiety contribute to enhanced metabolic stability and improved receptor affinity. Commonly employed in research settings for structure-activity relationship (SAR) studies aimed at optimizing drug candidates for improved potency and pharmacokinetic profiles.

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