4-(1-Methyl-4-piperidyl)phenylboronic Acid Pinacol Ester

≥95%

Reagent Code: #90321
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CAS Number 1247000-92-5

science Other reagents with same CAS 1247000-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.23 g/mol
Formula C₁₈H₂₈NO₂B
badge Registry Numbers
MDL Number MFCD18383496
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals, particularly those targeting neurological disorders. Its boronic ester group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex drug molecules. Additionally, it is employed in the development of bioactive compounds for research in medicinal chemistry, aiding in the discovery of new therapeutic agents. Its stability and reactivity make it valuable in creating diverse chemical libraries for high-throughput screening in drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,119.00
inventory 1g
10-20 days ฿17,487.00

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4-(1-Methyl-4-piperidyl)phenylboronic Acid Pinacol Ester
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals, particularly those targeting neurological disorders. Its boronic ester group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex drug molecules. Additionally, it is employed in the development of bioactive compounds for research in medicinal chemistry, aiding in the discovery of new therapeutic agen

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals, particularly those targeting neurological disorders. Its boronic ester group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex drug molecules. Additionally, it is employed in the development of bioactive compounds for research in medicinal chemistry, aiding in the discovery of new therapeutic agents. Its stability and reactivity make it valuable in creating diverse chemical libraries for high-throughput screening in drug discovery.

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