2-((cyclopropylaMino)Methyl)phenylboronic acid

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Reagent Code: #214612
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CAS Number 1335490-75-9

science Other reagents with same CAS 1335490-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.04 g/mol
Formula C₁₀H₁₄BNO₂
badge Registry Numbers
MDL Number MFCD28009331
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and kinase inhibitors. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing biaryl systems. Commonly employed in the preparation of drug candidates targeting cancer, inflammation, and viral infections. The cyclopropylamino moiety enhances metabolic stability and binding affinity in final drug molecules. Also utilized in the design of covalent inhibitors due to the reactivity of the boronic acid group with serine residues in enzymes.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿17,360.00

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2-((cyclopropylaMino)Methyl)phenylboronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and kinase inhibitors. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing biaryl systems. Commonly employed in the preparation of drug candidates targeting cancer, inflammation, and viral infections. The cyclopropylamino moiety enhances metabolic stability and binding affinity in final dru

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and kinase inhibitors. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing biaryl systems. Commonly employed in the preparation of drug candidates targeting cancer, inflammation, and viral infections. The cyclopropylamino moiety enhances metabolic stability and binding affinity in final drug molecules. Also utilized in the design of covalent inhibitors due to the reactivity of the boronic acid group with serine residues in enzymes.

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