Ethyl 2-((5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-yl)amino)acetate

96%

Reagent Code: #89605
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CAS Number 1202805-23-9

science Other reagents with same CAS 1202805-23-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.15 g/mol
Formula C₁₄H₂₂BN₃O₄
badge Registry Numbers
MDL Number MFCD12546563
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronate ester intermediate. Its pyrimidine ring and boronate ester functionality make it a valuable building block for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of drug candidates, enabling the formation of carbon-carbon bonds with high precision. Additionally, it finds use in material science for the preparation of organic electronic materials and polymers. Its stability and reactivity make it a versatile reagent in medicinal chemistry for designing and optimizing bioactive compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,971.00
inventory 250mg
10-20 days ฿3,339.00
inventory 1g
10-20 days ฿9,000.00

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Ethyl 2-((5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-yl)amino)acetate
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronate ester intermediate. Its pyrimidine ring and boronate ester functionality make it a valuable building block for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of drug candidates, enabling the formation of carbon-carbon bonds with high precision. Additionally, it finds use in material science for the preparation of organic electronic materials and polymers. Its stability and reactivity make it a versatile reagent in medicinal chemistry for designing and optimizing bioactive compounds.
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