2-(Ethyl-d5)-6-trifluoromethylpyridine-4-boronic acid

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Reagent Code: #91518
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CAS Number 2225173-11-3

science Other reagents with same CAS 2225173-11-3

blur_circular Chemical Specifications

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Weight 223.99957849 g/mol
Formula C₈H₄BD₅F₃NO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and 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 for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its deuterated ethyl group can be beneficial in studies involving isotopic labeling, aiding in metabolic research and the tracing of chemical pathways. Additionally, the trifluoromethyl group enhances the compound's reactivity and stability, making it suitable for creating compounds with specific electronic properties.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿86,080.00
inventory 25mg
10-20 days ฿223,800.00

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2-(Ethyl-d5)-6-trifluoromethylpyridine-4-boronic acid
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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 for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its deuterated ethyl group can be beneficial in studies involving isotopic labeling, aiding in metabolic research and the tracing of chemical pathways. Additionally, the trifluoromethyl group e

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 for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its deuterated ethyl group can be beneficial in studies involving isotopic labeling, aiding in metabolic research and the tracing of chemical pathways. Additionally, the trifluoromethyl group enhances the compound's reactivity and stability, making it suitable for creating compounds with specific electronic properties.

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