3-(2-Aminophenyl carbamoyl)phenylboronic acid

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Reagent Code: #44249
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CAS Number 1538623-29-8

science Other reagents with same CAS 1538623-29-8

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Weight 256.06492 g/mol
Formula C₁₃H₁₃BN₂O₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research due to its unique boronic acid and carbamoyl functional groups. It serves as a key intermediate in the development of boron-containing drugs, particularly in the synthesis of proteasome inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its boronic acid moiety enables it to form stable complexes with biomolecules, making it valuable in biochemical assays and drug delivery systems. Additionally, it is employed in the preparation of advanced materials, such as sensors and polymers, where its ability to interact with diols and other organic compounds is exploited for selective binding and recognition applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,488.00
inventory 1g
10-20 days ฿27,792.00
inventory 250mg
10-20 days ฿12,492.00

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3-(2-Aminophenyl carbamoyl)phenylboronic acid
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This compound is primarily utilized in organic synthesis and pharmaceutical research due to its unique boronic acid and carbamoyl functional groups. It serves as a key intermediate in the development of boron-containing drugs, particularly in the synthesis of proteasome inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its boronic acid moiety enables it to form stable complexes with biomolecules, making it valuable in biochemical assays and drug delivery systems. Additio

This compound is primarily utilized in organic synthesis and pharmaceutical research due to its unique boronic acid and carbamoyl functional groups. It serves as a key intermediate in the development of boron-containing drugs, particularly in the synthesis of proteasome inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its boronic acid moiety enables it to form stable complexes with biomolecules, making it valuable in biochemical assays and drug delivery systems. Additionally, it is employed in the preparation of advanced materials, such as sensors and polymers, where its ability to interact with diols and other organic compounds is exploited for selective binding and recognition applications.

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