2-Bromo-4-(cyclopropyl)pyrimidine-5-boronic acid

95%

Reagent Code: #91555
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CAS Number 2225176-67-8

science Other reagents with same CAS 2225176-67-8

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Weight 242.86562 g/mol
Formula C₇H₈BBrN₂O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic compounds, particularly in pharmaceutical research for drug development. It serves as a key intermediate in creating molecules with potential therapeutic applications. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the construction of diverse pyrimidine derivatives. These derivatives are often explored for their biological activity, including anticancer, antiviral, and anti-inflammatory properties. Its cyclopropyl group adds structural diversity, enhancing the compound's utility in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,520.00
inventory 25mg
10-20 days ฿45,060.00
inventory 100mg
10-20 days ฿135,200.00

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2-Bromo-4-(cyclopropyl)pyrimidine-5-boronic acid
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Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic compounds, particularly in pharmaceutical research for drug development. It serves as a key intermediate in creating molecules with potential therapeutic applications. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the construction of diverse pyrimidine derivatives. These derivatives are often explored for their biological activity, including anticancer, antiviral, and anti-inflammatory proper

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic compounds, particularly in pharmaceutical research for drug development. It serves as a key intermediate in creating molecules with potential therapeutic applications. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the construction of diverse pyrimidine derivatives. These derivatives are often explored for their biological activity, including anticancer, antiviral, and anti-inflammatory properties. Its cyclopropyl group adds structural diversity, enhancing the compound's utility in medicinal chemistry.

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