5-(Imidazol-1-yl)thiophene-2-boronic acid pinacol ester

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Reagent Code: #90831
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CAS Number 2223051-07-6

science Other reagents with same CAS 2223051-07-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.17756 g/mol
Formula C₁₃H₁₉BN₂O₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drugs targeting various diseases. Its boronic ester group makes it a valuable building block for creating carbon-carbon bonds, enabling the synthesis of biologically active compounds. Additionally, it is utilized in material science for the preparation of organic electronic materials, including polymers and small molecules for optoelectronic devices. Its stability and reactivity make it a preferred choice for researchers working on advanced chemical transformations.

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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-(Imidazol-1-yl)thiophene-2-boronic acid pinacol ester
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This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drugs targeting various diseases. Its boronic ester group makes it a valuable building block for creating carbon-carbon bonds, enabling the synthesis of biologically active compounds. Additionally, it is utilized in material science for

This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drugs targeting various diseases. Its boronic ester group makes it a valuable building block for creating carbon-carbon bonds, enabling the synthesis of biologically active compounds. Additionally, it is utilized in material science for the preparation of organic electronic materials, including polymers and small molecules for optoelectronic devices. Its stability and reactivity make it a preferred choice for researchers working on advanced chemical transformations.

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