4-Methyl-3-(3-(piperazin-1-yl)propoxy)phenylboronic acid

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Reagent Code: #90676
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CAS Number 1704064-32-3

science Other reagents with same CAS 1704064-32-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.16 g/mol
Formula C₁₄H₂₃BN₂O₃
badge Registry Numbers
MDL Number MFCD28384333
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various therapeutic agents. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex organic molecules. Additionally, it is employed in the development of enzyme inhibitors and receptor modulators, particularly in targeting neurological and oncological disorders. The piperazine moiety enhances its binding affinity to biological targets, making it useful in drug discovery and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿37,863.00

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4-Methyl-3-(3-(piperazin-1-yl)propoxy)phenylboronic acid
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various therapeutic agents. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex organic molecules. Additionally, it is employed in the development of enzyme inhibitors and receptor modulators, particularly in targeting neurological and oncological disorders. The piperazine moiety enhances its binding affinity to biological targets, mak

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various therapeutic agents. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex organic molecules. Additionally, it is employed in the development of enzyme inhibitors and receptor modulators, particularly in targeting neurological and oncological disorders. The piperazine moiety enhances its binding affinity to biological targets, making it useful in drug discovery and medicinal chemistry.

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