4-(4-Boc-piperazino)phenylboronic Acid Pinacol Ester

≥97%

Reagent Code: #90420
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CAS Number 470478-90-1

science Other reagents with same CAS 470478-90-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 388.31 g/mol
Formula C₂₁H₃₃N₂O₄B
badge Registry Numbers
MDL Number MFCD06411544
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex molecules. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The Boc-protected piperazine moiety enhances its stability and allows for selective deprotection, enabling its use in the development of bioactive compounds and drug candidates. Additionally, it is employed in the preparation of polymers and functionalized materials, where its structural properties contribute to tailored material characteristics.

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Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,449.00
inventory 1g
10-20 days ฿4,068.00

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4-(4-Boc-piperazino)phenylboronic Acid Pinacol Ester
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex molecules. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The Boc-protected piperazine moiety enhances its stability and allows for selective deprotection, enabling its use in the development of bioactive compounds and

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex molecules. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The Boc-protected piperazine moiety enhances its stability and allows for selective deprotection, enabling its use in the development of bioactive compounds and drug candidates. Additionally, it is employed in the preparation of polymers and functionalized materials, where its structural properties contribute to tailored material characteristics.

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