2-(1-(Ethylsulfonyl)-3-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-1H-Pyrazol-1-Yl)Azetidin-3-Yl)Acetonitrile

95%

Reagent Code: #185658
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CAS Number 1919837-50-5

science Other reagents with same CAS 1919837-50-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 380.27 g/mol
Formula C₁₆H₂₅BN₄O₄S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, especially in the development of kinase inhibitors for targeted cancer therapies. Its structure supports cross-coupling reactions via the boronate ester group, enabling efficient construction of complex drug molecules. Commonly employed in Suzuki-Miyaura coupling reactions during medicinal chemistry research to generate diverse analogs for structure-activity relationship studies. Its nitrile and sulfone functionalities enhance binding selectivity and metabolic stability in final active pharmaceutical ingredients. Widely applied in late-stage functionalization due to its compatibility with various reaction conditions, making it valuable in oncology drug discovery programs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,700.00
inventory 5g
10-20 days ฿6,610.00
2-(1-(Ethylsulfonyl)-3-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-1H-Pyrazol-1-Yl)Azetidin-3-Yl)Acetonitrile
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, especially in the development of kinase inhibitors for targeted cancer therapies. Its structure supports cross-coupling reactions via the boronate ester group, enabling efficient construction of complex drug molecules. Commonly employed in Suzuki-Miyaura coupling reactions during medicinal chemistry research to generate diverse analogs for structure-activity relationship studies. Its nitrile and sulfone functionalities enh

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, especially in the development of kinase inhibitors for targeted cancer therapies. Its structure supports cross-coupling reactions via the boronate ester group, enabling efficient construction of complex drug molecules. Commonly employed in Suzuki-Miyaura coupling reactions during medicinal chemistry research to generate diverse analogs for structure-activity relationship studies. Its nitrile and sulfone functionalities enhance binding selectivity and metabolic stability in final active pharmaceutical ingredients. Widely applied in late-stage functionalization due to its compatibility with various reaction conditions, making it valuable in oncology drug discovery programs.

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