2-(Methyl-d3)-6-trifluoromethylpyridine-4-boronic acid

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Reagent Code: #91546
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CAS Number 2225174-44-5

science Other reagents with same CAS 2225174-44-5

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Weight 207.960674934 g/mol
Formula C₇H₄BD₃F₃NO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable boronic acid reagent for introducing the 2-(methyl-d3)-6-trifluoromethylpyridine moiety into complex molecules. Its deuterated methyl group makes it useful in isotopic labeling studies, aiding in the tracking and analysis of chemical pathways or metabolic processes. Additionally, the trifluoromethyl group enhances the lipophilicity and stability of the resulting compounds, making it relevant in pharmaceutical and agrochemical research for developing bioactive molecules. Its application is also seen in material science for creating advanced organic materials with specific electronic or structural 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-(Methyl-d3)-6-trifluoromethylpyridine-4-boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable boronic acid reagent for introducing the 2-(methyl-d3)-6-trifluoromethylpyridine moiety into complex molecules. Its deuterated methyl group makes it useful in isotopic labeling studies, aiding in the tracking and analysis of chemical pathways or metabolic processes. Additionally, the trifluoromethyl group enhances the lipophilicity and stability o

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable boronic acid reagent for introducing the 2-(methyl-d3)-6-trifluoromethylpyridine moiety into complex molecules. Its deuterated methyl group makes it useful in isotopic labeling studies, aiding in the tracking and analysis of chemical pathways or metabolic processes. Additionally, the trifluoromethyl group enhances the lipophilicity and stability of the resulting compounds, making it relevant in pharmaceutical and agrochemical research for developing bioactive molecules. Its application is also seen in material science for creating advanced organic materials with specific electronic or structural properties.

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