5-(3-Methoxyphenyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90780
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CAS Number 1402227-47-7

science Other reagents with same CAS 1402227-47-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.23812 g/mol
Formula C₁₇H₂₃BO₄S
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 the Suzuki-Miyaura reaction. It serves as a key intermediate in the construction of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Additionally, it is used in the synthesis of conjugated polymers and organic electronic materials due to its ability to introduce thiophene-based structures, which are essential in optoelectronic applications.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿19,800.00

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5-(3-Methoxyphenyl)thiophene-2-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the construction of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Ad

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the construction of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Additionally, it is used in the synthesis of conjugated polymers and organic electronic materials due to its ability to introduce thiophene-based structures, which are essential in optoelectronic applications.

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