2-(5-Borono-2-pyrimidinyl)imidodicarbonic acid 1,3-bis(tert-butyl) ester

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Reagent Code: #41789
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CAS Number 1360950-40-8

science Other reagents with same CAS 1360950-40-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.15 g/mol
Formula C₁₄H₂₂BN₃O₆
badge Registry Numbers
MDL Number MFCD16876794
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate, particularly in the development of pharmaceuticals and bioactive compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in drug discovery and material science. The tert-butyl ester groups provide stability and protection during synthetic processes, enabling selective reactions in complex molecular frameworks. It is also explored in the preparation of boron-containing compounds for potential applications in cancer therapy and as enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,295.00
inventory 1g
10-20 days ฿8,991.00
inventory 100mg
10-20 days ฿1,224.00

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2-(5-Borono-2-pyrimidinyl)imidodicarbonic acid 1,3-bis(tert-butyl) ester
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This chemical is primarily utilized in organic synthesis as a versatile intermediate, particularly in the development of pharmaceuticals and bioactive compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in drug discovery and material science. The tert-butyl ester groups provide stability and protection during synthetic processes, enabling selective reactions in complex molecular frameworks. It is also e

This chemical is primarily utilized in organic synthesis as a versatile intermediate, particularly in the development of pharmaceuticals and bioactive compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in drug discovery and material science. The tert-butyl ester groups provide stability and protection during synthetic processes, enabling selective reactions in complex molecular frameworks. It is also explored in the preparation of boron-containing compounds for potential applications in cancer therapy and as enzyme inhibitors.

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