(2,4-Dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)boronic acid

98%

Reagent Code: #180084
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CAS Number 70523-22-7

science Other reagents with same CAS 70523-22-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.91 g/mol
Formula C₄H₅BN₂O₄
badge Registry Numbers
MDL Number MFCD01318983
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nucleoside analogs and boron-containing drugs. Its structure allows for Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex molecules for medicinal chemistry. Commonly employed in research settings to design inhibitors targeting enzymes involved in metabolic and oncological pathways. Also explored in the preparation of bioactive molecules with antiviral and anticancer properties due to its ability to mimic pyrimidine bases while introducing boronic acid functionality for enhanced binding or targeting.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,860.00
inventory 250mg
10-20 days ฿11,650.00
inventory 1g
10-20 days ฿30,270.00

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(2,4-Dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nucleoside analogs and boron-containing drugs. Its structure allows for Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex molecules for medicinal chemistry. Commonly employed in research settings to design inhibitors targeting enzymes involved in metabolic and oncological pathways. Also explored in the preparation of bioactive molecules with antiviral and anticancer prop

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nucleoside analogs and boron-containing drugs. Its structure allows for Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex molecules for medicinal chemistry. Commonly employed in research settings to design inhibitors targeting enzymes involved in metabolic and oncological pathways. Also explored in the preparation of bioactive molecules with antiviral and anticancer properties due to its ability to mimic pyrimidine bases while introducing boronic acid functionality for enhanced binding or targeting.

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