tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrolidine-1-carboxylate

98%

Reagent Code: #51652
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CAS Number 1312712-22-3

science Other reagents with same CAS 1312712-22-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.2100 g/mol
Formula C₁₅H₂₈BNO₄
badge Registry Numbers
MDL Number MFCD12032619
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It is valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group makes it a key reagent for introducing pyrrolidine moieties into target compounds. Additionally, it is utilized in the preparation of bioactive molecules and in medicinal chemistry research for drug discovery and development. Its stability and reactivity make it a preferred choice for constructing nitrogen-containing heterocycles in various synthetic pathways.

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inventory 100mg
10-20 days ฿2,088.00

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tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrolidine-1-carboxylate
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This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It is valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group makes it a key reagent for introducing pyrrolidine moieties into target compounds. Additionally, it is utilized in the preparation of bioactive molecules and in medicinal chemistry

This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It is valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group makes it a key reagent for introducing pyrrolidine moieties into target compounds. Additionally, it is utilized in the preparation of bioactive molecules and in medicinal chemistry research for drug discovery and development. Its stability and reactivity make it a preferred choice for constructing nitrogen-containing heterocycles in various synthetic pathways.

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