5-(2-Chloropyrimidin-4-yl)thiophene-2-boronic acid

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Reagent Code: #92232
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CAS Number 2225176-24-7

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blur_circular Chemical Specifications

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Weight 240.47444 g/mol
Formula C₈H₆BClN₂O₂S
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the pharmaceutical industry. It is valuable in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct carbon-carbon bonds efficiently. This enables the development of biologically active compounds, including potential drug candidates. Its pyrimidine and thiophene moieties make it suitable for creating heterocyclic structures, which are common in medicinal chemistry. Additionally, it is employed in material science for the synthesis of organic electronic materials, contributing to the development of advanced technologies like organic light-emitting diodes (OLEDs) and semiconductors.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿13,400.00
inventory 25mg
10-20 days ฿40,200.00
inventory 100mg
10-20 days ฿120,600.00

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5-(2-Chloropyrimidin-4-yl)thiophene-2-boronic acid
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Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the pharmaceutical industry. It is valuable in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct carbon-carbon bonds efficiently. This enables the development of biologically active compounds, including potential drug candidates. Its pyrimidine and thiophene moieties make it suitable for creating heterocyclic structures, which are common in medicinal chemistry. Additionally, it

Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the pharmaceutical industry. It is valuable in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct carbon-carbon bonds efficiently. This enables the development of biologically active compounds, including potential drug candidates. Its pyrimidine and thiophene moieties make it suitable for creating heterocyclic structures, which are common in medicinal chemistry. Additionally, it is employed in material science for the synthesis of organic electronic materials, contributing to the development of advanced technologies like organic light-emitting diodes (OLEDs) and semiconductors.

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