(2-Methyl-5-morpholino-d11)-thiophene-3-boronic acid pinacol ester

95%

Reagent Code: #89028
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CAS Number 2223032-40-2

science Other reagents with same CAS 2223032-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.315019558 g/mol
Formula C₁₅H₁₅BD₁₁NO₄S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in advanced organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions, where it acts as a boronic ester reagent. Its deuterated structure makes it valuable in isotopic labeling studies, enabling researchers to track molecular pathways and mechanisms in pharmaceuticals and biochemical research. The morpholino group enhances its solubility and stability, making it suitable for applications in medicinal chemistry for the development of drug candidates. Additionally, its thiophene moiety is beneficial in materials science for designing organic semiconductors and conductive polymers.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿269,660.00
inventory 25mg
10-20 days ฿699,980.00

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(2-Methyl-5-morpholino-d11)-thiophene-3-boronic acid pinacol ester
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This compound is primarily utilized in advanced organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions, where it acts as a boronic ester reagent. Its deuterated structure makes it valuable in isotopic labeling studies, enabling researchers to track molecular pathways and mechanisms in pharmaceuticals and biochemical research. The morpholino group enhances its solubility and stability, making it suitable for applications in medicinal chemistry for the development of d

This compound is primarily utilized in advanced organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions, where it acts as a boronic ester reagent. Its deuterated structure makes it valuable in isotopic labeling studies, enabling researchers to track molecular pathways and mechanisms in pharmaceuticals and biochemical research. The morpholino group enhances its solubility and stability, making it suitable for applications in medicinal chemistry for the development of drug candidates. Additionally, its thiophene moiety is beneficial in materials science for designing organic semiconductors and conductive polymers.

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