(6-(methyl-d3)-5-(propan-2-yl-d7)pyridin-3-yl-2,4-d2)boronic acid

95%

Reagent Code: #91370
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CAS Number 2241870-48-2

science Other reagents with same CAS 2241870-48-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.11507778 g/mol
Formula C₁₇H₉BCl₂D₁₀NO₅
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research as a deuterated boronic acid derivative. Its deuterated structure makes it valuable in studies involving isotopic labeling, particularly in the development of deuterated drugs, where it helps in tracking metabolic pathways and understanding drug behavior in biological systems. It is also employed in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds, due to its boronic acid functional group. Additionally, its isotopic labeling aids in NMR spectroscopy, providing clearer and more precise analytical data for complex molecular structures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿154,420.00
25mg
10-20 days ฿463,260.00
(6-(methyl-d3)-5-(propan-2-yl-d7)pyridin-3-yl-2,4-d2)boronic acid
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This compound is primarily utilized in organic synthesis and pharmaceutical research as a deuterated boronic acid derivative. Its deuterated structure makes it valuable in studies involving isotopic labeling, particularly in the development of deuterated drugs, where it helps in tracking metabolic pathways and understanding drug behavior in biological systems. It is also employed in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds, due to its boronic acid functional g

This compound is primarily utilized in organic synthesis and pharmaceutical research as a deuterated boronic acid derivative. Its deuterated structure makes it valuable in studies involving isotopic labeling, particularly in the development of deuterated drugs, where it helps in tracking metabolic pathways and understanding drug behavior in biological systems. It is also employed in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds, due to its boronic acid functional group. Additionally, its isotopic labeling aids in NMR spectroscopy, providing clearer and more precise analytical data for complex molecular structures.

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