(R)-1-((R)-1-phenylethyl)-2-(trifluoromethyl)-2,3-dihydropyridin-4(1H)-one

Reagent Code: #37302
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CAS Number 577692-44-5

science Other reagents with same CAS 577692-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.26 g/mol
Formula C₁₄H₁₄F₃NO
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its chiral structure makes it valuable for the development of enantioselective drugs, particularly those targeting neurological disorders and inflammatory diseases. The trifluoromethyl group enhances the compound's metabolic stability and bioavailability, making it a preferred choice in drug design. Additionally, it serves as a building block in the creation of complex organic frameworks for research in asymmetric catalysis, enabling the production of high-purity chiral compounds for pharmaceutical applications.

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inventory 200mg
10-20 days ฿9,000.00

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(R)-1-((R)-1-phenylethyl)-2-(trifluoromethyl)-2,3-dihydropyridin-4(1H)-one
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its chiral structure makes it valuable for the development of enantioselective drugs, particularly those targeting neurological disorders and inflammatory diseases. The trifluoromethyl group enhances the compound's metabolic stability and bioavailability, making it a preferred choice in drug design. Additionally, it serves as a building block in the creation of

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its chiral structure makes it valuable for the development of enantioselective drugs, particularly those targeting neurological disorders and inflammatory diseases. The trifluoromethyl group enhances the compound's metabolic stability and bioavailability, making it a preferred choice in drug design. Additionally, it serves as a building block in the creation of complex organic frameworks for research in asymmetric catalysis, enabling the production of high-purity chiral compounds for pharmaceutical applications.

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