4-Amino-2-phenylpyrimidine-5-boronic acid pinacol ester

95%

Reagent Code: #60865
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CAS Number 2223050-34-6

science Other reagents with same CAS 2223050-34-6

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scatter_plot Molecular Information
Weight 315.17518 g/mol
Formula C₁₆H₂₂BN₃O₃
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceutical research for developing new drugs. The boronic ester group facilitates the formation of carbon-carbon bonds, making it essential in constructing molecules with potential therapeutic properties. Additionally, it serves as a key intermediate in the synthesis of various heterocyclic compounds, which are often explored for their biological activities. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry and material science applications.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,612.00
inventory 25mg
10-20 days ฿21,600.00

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4-Amino-2-phenylpyrimidine-5-boronic acid pinacol ester
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceutical research for developing new drugs. The boronic ester group facilitates the formation of carbon-carbon bonds, making it essential in constructing molecules with potential therapeutic properties. Additionally, it serves as a key intermediate in the synthesis of various heterocyclic compounds, which are often explored for their biological acti

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceutical research for developing new drugs. The boronic ester group facilitates the formation of carbon-carbon bonds, making it essential in constructing molecules with potential therapeutic properties. Additionally, it serves as a key intermediate in the synthesis of various heterocyclic compounds, which are often explored for their biological activities. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry and material science applications.

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