(2-Methyl-5-pyrrolidino-d11)-furan-3-boronic acid pinacol ester

95%

Reagent Code: #89029
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CAS Number 2223051-03-2

science Other reagents with same CAS 2223051-03-2

blur_circular Chemical Specifications

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Weight 306.250019558 g/mol
Formula C₁₅H₁₅BD₁₁NO₄
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 ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled pyrrolidine moiety enhances its use in mechanistic studies and isotopic labeling, aiding in the tracking of chemical pathways and metabolic processes. Additionally, it serves as a key intermediate in the development of deuterated compounds for research in drug discovery and development.

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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-Methyl-5-pyrrolidino-d11)-furan-3-boronic acid pinacol ester
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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 ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled pyrrolidine moiety enhances its use in mechanistic studies and isotopic labeling, aiding in the tracking of chemical pathways and metabolic processes. 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 ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled pyrrolidine moiety enhances its use in mechanistic studies and isotopic labeling, aiding in the tracking of chemical pathways and metabolic processes. Additionally, it serves as a key intermediate in the development of deuterated compounds for research in drug discovery and development.

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