5-(Morpholino)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90836
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CAS Number 2223033-16-5

science Other reagents with same CAS 2223033-16-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.22066 g/mol
Formula C₁₄H₂₄BNO₄S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality enables the formation of carbon-carbon bonds, making it valuable for creating diverse organic frameworks. Additionally, it is employed in material science for developing advanced polymers and electronic materials due to its ability to introduce thiophene and morpholine moieties, which can enhance material properties. Its applications also extend to the synthesis of bioactive compounds and functionalized materials for research and industrial purposes.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,552.00
inventory 100mg
10-20 days ฿46,602.00

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5-(Morpholino)thiophene-2-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality enables the formation of carbon-carbon bonds, making it valuable for creating diverse organic frameworks. Additionally, it is employed in material science for developing advanced polymers and electronic materials d

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality enables the formation of carbon-carbon bonds, making it valuable for creating diverse organic frameworks. Additionally, it is employed in material science for developing advanced polymers and electronic materials due to its ability to introduce thiophene and morpholine moieties, which can enhance material properties. Its applications also extend to the synthesis of bioactive compounds and functionalized materials for research and industrial purposes.

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