2-(Ethyl-d5)-4-chloropyrimidine-5-boronic acid

95%

Reagent Code: #89653
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CAS Number 2225178-91-4

science Other reagents with same CAS 2225178-91-4

blur_circular Chemical Specifications

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Weight 191.43472889 g/mol
Formula C₆H₃BClD₅N₂O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable for constructing complex molecules, especially in pharmaceutical research. The deuterated ethyl group (ethyl-d5) enhances its use in studies involving isotopic labeling, which is crucial for tracking and understanding metabolic pathways and drug mechanisms. Additionally, its chloropyrimidine moiety allows for further functionalization, making it a versatile intermediate in the development of bioactive compounds and materials.

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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-(Ethyl-d5)-4-chloropyrimidine-5-boronic acid
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This compound is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable for constructing complex molecules, especially in pharmaceutical research. The deuterated ethyl group (ethyl-d5) enhances its use in studies involving isotopic labeling, which is crucial for tracking and understanding metabolic pathways and drug mechanisms. Add

This compound is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable for constructing complex molecules, especially in pharmaceutical research. The deuterated ethyl group (ethyl-d5) enhances its use in studies involving isotopic labeling, which is crucial for tracking and understanding metabolic pathways and drug mechanisms. Additionally, its chloropyrimidine moiety allows for further functionalization, making it a versatile intermediate in the development of bioactive compounds and materials.

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