[2-Methyl-5-(iso-propyl)-d10]-thiophene-3-boronic acid pinacol ester

95%

Reagent Code: #91047
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CAS Number 2223054-54-2

science Other reagents with same CAS 2223054-54-2

blur_circular Chemical Specifications

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Weight 294.28411778 g/mol
Formula C₁₄H₁₅BD₁₀O₃S
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 such as Suzuki-Miyaura reactions, where it acts as a key building block for creating complex organic molecules. Its boronic ester functional group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuteration (d10) in the structure enhances its utility in research involving isotopic labeling, aiding in mechanistic studies and metabolic pathway analysis. Additionally, its thiophene moiety contributes to its application in the synthesis of conjugated polymers and organic electronic materials, which are essential in the production of organic light-emitting diodes (OLEDs) and organic photovoltaics.

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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-(iso-propyl)-d10]-thiophene-3-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions, where it acts as a key building block for creating complex organic molecules. Its boronic ester functional group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuteration (d10) in the structure enhances its utility in research involving isotopic labeling, aiding in

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions, where it acts as a key building block for creating complex organic molecules. Its boronic ester functional group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuteration (d10) in the structure enhances its utility in research involving isotopic labeling, aiding in mechanistic studies and metabolic pathway analysis. Additionally, its thiophene moiety contributes to its application in the synthesis of conjugated polymers and organic electronic materials, which are essential in the production of organic light-emitting diodes (OLEDs) and organic photovoltaics.

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