6-Methyl-2-(thiophen-3-yl)-1,3,6,2-dioxazaborocane-4,8-dione

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Reagent Code: #208543
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CAS Number 1604722-27-1

science Other reagents with same CAS 1604722-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.06 g/mol
Formula C₉H₁₀BNO₄S
badge Registry Numbers
MDL Number MFCD27980597
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of boron-containing pharmaceuticals, particularly in the development of protease inhibitors. Its unique heterocyclic structure with a boron atom enables selective binding to enzyme active sites, making it valuable in drug discovery for oncology and antiviral therapies. Also employed in asymmetric synthesis due to its chiral boron center, facilitating the production of enantiomerically pure compounds. Additionally, it serves as a building block in materials science for creating novel boron-based polymers with potential applications in optoelectronics.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,220.00
inventory 5g
10-20 days ฿18,260.00
inventory 25g
10-20 days ฿63,900.00

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6-Methyl-2-(thiophen-3-yl)-1,3,6,2-dioxazaborocane-4,8-dione
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Used as a key intermediate in the synthesis of boron-containing pharmaceuticals, particularly in the development of protease inhibitors. Its unique heterocyclic structure with a boron atom enables selective binding to enzyme active sites, making it valuable in drug discovery for oncology and antiviral therapies. Also employed in asymmetric synthesis due to its chiral boron center, facilitating the production of enantiomerically pure compounds. Additionally, it serves as a building block in materials scie

Used as a key intermediate in the synthesis of boron-containing pharmaceuticals, particularly in the development of protease inhibitors. Its unique heterocyclic structure with a boron atom enables selective binding to enzyme active sites, making it valuable in drug discovery for oncology and antiviral therapies. Also employed in asymmetric synthesis due to its chiral boron center, facilitating the production of enantiomerically pure compounds. Additionally, it serves as a building block in materials science for creating novel boron-based polymers with potential applications in optoelectronics.

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