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

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Reagent Code: #90765
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CAS Number 2223039-66-3

science Other reagents with same CAS 2223039-66-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.20414 g/mol
Formula C₁₄H₂₁BN₂O₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group, attached to a thiophene ring substituted with a 2-methylimidazol-1-yl group, enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds in heteroaromatic systems. Additionally, it is employed in material science for synthesizing organic electronic materials, including polymers and small molecules for optoelectronic devices. Its stability and reactivity make it a valuable component in research and industrial applications.

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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-(2-Methylimidazol-1-yl)thiophene-2-boronic acid pinacol ester
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group, attached to a thiophene ring substituted with a 2-methylimidazol-1-yl group, enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds in heteroaromatic systems. Addition

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group, attached to a thiophene ring substituted with a 2-methylimidazol-1-yl group, enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds in heteroaromatic systems. Additionally, it is employed in material science for synthesizing organic electronic materials, including polymers and small molecules for optoelectronic devices. Its stability and reactivity make it a valuable component in research and industrial applications.

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