6-((tert-butyldimethylsilyl)oxy)benzofuran-3(2H)-one

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Reagent Code: #124438
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CAS Number 299912-77-9

science Other reagents with same CAS 299912-77-9

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Weight 264.39 g/mol
Formula C₁₄H₂₀O₃Si
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MDL Number MFCD22393527
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description Product Description

This compound is primarily utilized in organic synthesis as a protected intermediate for the construction of complex molecules, particularly in pharmaceutical research. Its tert-butyldimethylsilyl (TBDMS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. It is often employed in the development of benzofuran-based compounds, which are known for their biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Additionally, its stability and ease of deprotection make it a valuable tool in the synthesis of natural products and bioactive molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿2,700.00

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6-((tert-butyldimethylsilyl)oxy)benzofuran-3(2H)-one
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This compound is primarily utilized in organic synthesis as a protected intermediate for the construction of complex molecules, particularly in pharmaceutical research. Its tert-butyldimethylsilyl (TBDMS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. It is often employed in the development of benzofuran-based compounds, which are known for their biological activities, including anti-inflammatory, antimicrobial, and anticancer

This compound is primarily utilized in organic synthesis as a protected intermediate for the construction of complex molecules, particularly in pharmaceutical research. Its tert-butyldimethylsilyl (TBDMS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. It is often employed in the development of benzofuran-based compounds, which are known for their biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Additionally, its stability and ease of deprotection make it a valuable tool in the synthesis of natural products and bioactive molecules.

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