(4S,5R)-2-(6-Cyclopropylpyridin-2-yl)-4,5-diphenyl-4,5-dihydrooxazole

97%

Reagent Code: #237473
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CAS Number 2828438-63-5

science Other reagents with same CAS 2828438-63-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 340.42 g/mol
Formula C₂₃H₂₀N₂O
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its chiral oxazole core enables selective interactions with biological targets, enhancing drug efficacy and reducing off-target effects. Commonly employed in research settings to optimize lead compounds due to its structural stability and ability to mimic peptide motifs. Also utilized in asymmetric synthesis to introduce stereochemical control in complex molecule construction.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,900.00
inventory 250mg
10-20 days ฿19,050.00
inventory 1g
10-20 days ฿70,160.00
(4S,5R)-2-(6-Cyclopropylpyridin-2-yl)-4,5-diphenyl-4,5-dihydrooxazole
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its chiral oxazole core enables selective interactions with biological targets, enhancing drug efficacy and reducing off-target effects. Commonly employed in research settings to optimize lead compounds due to its structural stability and ability to mimic peptide motifs. Also utilized in asymmetric synthesis to introduce stereochemical control in comple

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its chiral oxazole core enables selective interactions with biological targets, enhancing drug efficacy and reducing off-target effects. Commonly employed in research settings to optimize lead compounds due to its structural stability and ability to mimic peptide motifs. Also utilized in asymmetric synthesis to introduce stereochemical control in complex molecule construction.

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