[2-Methyl-5-(sec-butyl)-d12]-pyridine-3-boronic acid

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Reagent Code: #92581
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CAS Number 2225152-44-1

science Other reagents with same CAS 2225152-44-1

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inventory_2 Storage & Handling
Storage -20℃, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled structure (d12) is especially useful in research applications, such as isotopic labeling studies, to track and analyze chemical reactions or metabolic pathways. Its specific structure, with a sec-butyl group, allows for tailored reactivity in synthesizing compounds with specific steric or electronic properties.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿269,620.00
inventory 25mg
10-20 days ฿720,000.00

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[2-Methyl-5-(sec-butyl)-d12]-pyridine-3-boronic acid
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled structure (d12) is especially useful in research applications, such as isotopic labeling studies, to track and analyze chemical reactions or metabolic pathways. Its specif

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled structure (d12) is especially useful in research applications, such as isotopic labeling studies, to track and analyze chemical reactions or metabolic pathways. Its specific structure, with a sec-butyl group, allows for tailored reactivity in synthesizing compounds with specific steric or electronic properties.

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