(4-Chloro-3-(4-hydroxypiperidine-1-carbonyl)phenyl)boronic acid

98%

Reagent Code: #89304
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CAS Number 1704080-30-7

science Other reagents with same CAS 1704080-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.52 g/mol
Formula C₁₂H₁₅BClNO₄
badge Registry Numbers
MDL Number MFCD28400400
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the hydroxypiperidine moiety can enhance the compound’s solubility and bioavailability, making it a potential intermediate in the development of drug candidates. Its specific structure may also be explored for targeting enzymes or receptors in biochemical studies.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿110,000.00
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(4-Chloro-3-(4-hydroxypiperidine-1-carbonyl)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the hydroxypiperidine moiety can enhance the compound’s solubility and bioavailability, making it a potential intermediate in the dev

This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the hydroxypiperidine moiety can enhance the compound’s solubility and bioavailability, making it a potential intermediate in the development of drug candidates. Its specific structure may also be explored for targeting enzymes or receptors in biochemical studies.

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