4-[(piperazin-1-yl)methyl]phenylboronic acid hydrochloride

95%

Reagent Code: #226475
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CAS Number 2096338-77-9

science Other reagents with same CAS 2096338-77-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.54 g/mol
Formula C₁₁H₁₈BClN₂O₂
badge Registry Numbers
MDL Number MFCD18783116
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical intermediates. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to its piperazine and boronic acid functional groups. Its structure supports conjugation with aromatic systems, making it valuable in medicinal chemistry for designing drug candidates targeting cancer and inflammatory diseases. Also utilized in the preparation of sensors and functional materials where boronic acid groups act as glucose recognition elements.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿24,000.00
inventory 1g
10-20 days ฿48,000.00

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4-[(piperazin-1-yl)methyl]phenylboronic acid hydrochloride
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Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical intermediates. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to its piperazine and boronic acid functional groups. Its structure supports conjugation with aromatic systems, making it valuable in medicinal chemistry for designing drug candidates targeting cancer and inflammatory diseases. Also utilized i

Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical intermediates. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to its piperazine and boronic acid functional groups. Its structure supports conjugation with aromatic systems, making it valuable in medicinal chemistry for designing drug candidates targeting cancer and inflammatory diseases. Also utilized in the preparation of sensors and functional materials where boronic acid groups act as glucose recognition elements.

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