(2-Methyl-5-ethyl-d8)-thiophene-3-boronic acid pinacol ester

95%

Reagent Code: #89026
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CAS Number 2223032-30-0

science Other reagents with same CAS 2223032-30-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.245214224 g/mol
Formula C₁₃H₁₅BD₈O₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily 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 development of pharmaceuticals and agrochemicals. Its deuterated form (d8) makes it valuable in isotopic labeling studies, aiding in the tracing and analysis of reaction mechanisms or metabolic pathways. Additionally, it is utilized in the synthesis of advanced materials, including organic semiconductors and polymers, due to its ability to introduce thiophene-based structures, which are essential for electronic and optoelectronic applications.

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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-ethyl-d8)-thiophene-3-boronic acid pinacol ester
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This compound is primarily 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 development of pharmaceuticals and agrochemicals. Its deuterated form (d8) makes it valuable in isotopic labeling studies, aiding in the tracing and analysis of reaction mechanisms or metabolic pathways. Additionally, it is utilized in the synthesis of advanced materials, including organic sem

This compound is primarily 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 development of pharmaceuticals and agrochemicals. Its deuterated form (d8) makes it valuable in isotopic labeling studies, aiding in the tracing and analysis of reaction mechanisms or metabolic pathways. Additionally, it is utilized in the synthesis of advanced materials, including organic semiconductors and polymers, due to its ability to introduce thiophene-based structures, which are essential for electronic and optoelectronic applications.

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