tert-Butyl3-(4-Chlorobenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate

≥90%(HPLC)

Reagent Code: #154875
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CAS Number 2507954-86-9

science Other reagents with same CAS 2507954-86-9

blur_circular Chemical Specifications

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Weight 407.74 g/mol
Formula C₂₁H₃₁BClNO₄
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical development. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in constructing azetidine-containing drug candidates. The tert-butyloxycarbonyl (Boc) protecting group ensures stability during reactions and can be easily removed later in the synthesis. Commonly applied in medicinal chemistry for developing bioactive compounds with improved metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,890.00

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tert-Butyl3-(4-Chlorobenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical development. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in constructing azetidine-containing drug candidates. The tert-butyloxycarbonyl (Boc) protecting group ensures stability during reactions and can be easily removed later in the synthesis. Commonly applied in medicinal chemistry for d

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical development. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in constructing azetidine-containing drug candidates. The tert-butyloxycarbonyl (Boc) protecting group ensures stability during reactions and can be easily removed later in the synthesis. Commonly applied in medicinal chemistry for developing bioactive compounds with improved metabolic stability and binding affinity.

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