4-((4-fluoro-2-(4,4,5,5-tetraMethyl-1,3-dioxolan-2-yl)phenyl)sulfonyl)Morpholine

98%

Reagent Code: #207557
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CAS Number 1704069-32-8

science Other reagents with same CAS 1704069-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 371.24 g/mol
Formula C₁₆H₂₃BFNO₅S
badge Registry Numbers
MDL Number MFCD29108278
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure supports the development of sulfone-based molecules with potential antitumor and anti-inflammatory properties. The boronate ester group enables cross-coupling reactions, making it valuable in medicinal chemistry for building complex aromatic systems. Commonly employed in Suzuki-Miyaura coupling to create novel drug candidates. Also utilized in the preparation of kinase inhibitors and other targeted therapies in oncology research.

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inventory 1g
10-20 days ฿64,020.00

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4-((4-fluoro-2-(4,4,5,5-tetraMethyl-1,3-dioxolan-2-yl)phenyl)sulfonyl)Morpholine
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure supports the development of sulfone-based molecules with potential antitumor and anti-inflammatory properties. The boronate ester group enables cross-coupling reactions, making it valuable in medicinal chemistry for building complex aromatic systems. Commonly employed in Suzuki-Miyaura coupling to create novel drug candidates. Also utilized in the preparation of kinase inhibit

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure supports the development of sulfone-based molecules with potential antitumor and anti-inflammatory properties. The boronate ester group enables cross-coupling reactions, making it valuable in medicinal chemistry for building complex aromatic systems. Commonly employed in Suzuki-Miyaura coupling to create novel drug candidates. Also utilized in the preparation of kinase inhibitors and other targeted therapies in oncology research.

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