(tetrahydrofuran-3-yl-d7)boronic acid

95%

Reagent Code: #89406
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CAS Number 2241870-26-6

science Other reagents with same CAS 2241870-26-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 122.966592446 g/mol
Formula C₄H₂BD₇O₃
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions. Its deuterated form allows for studies in isotopic labeling, aiding in the tracking and analysis of reaction mechanisms and pathways. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of complex molecules where precise control over molecular structure is crucial. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of various organic compounds, including polymers and fine chemicals.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿168,000.00
inventory 25mg
10-20 days ฿324,000.00
inventory 100mg
10-20 days ฿972,000.00
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(tetrahydrofuran-3-yl-d7)boronic acid
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Used primarily in organic synthesis, this compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions. Its deuterated form allows for studies in isotopic labeling, aiding in the tracking and analysis of reaction mechanisms and pathways. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of complex molecules where precise control over molecular structure is crucial. Its boronic acid group facilitates the formation of carbon-carbon bonds, making

Used primarily in organic synthesis, this compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions. Its deuterated form allows for studies in isotopic labeling, aiding in the tracking and analysis of reaction mechanisms and pathways. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of complex molecules where precise control over molecular structure is crucial. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of various organic compounds, including polymers and fine chemicals.

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