N-(2-Hydroxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

98%

Reagent Code: #121338
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CAS Number 1073353-51-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.15 g/mol
Formula C₁₅H₂₂BNO₄
badge Registry Numbers
MDL Number MFCD06795648
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of boron-containing compounds. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a precursor for developing bioconjugates and probes in biochemical research, particularly in labeling and imaging applications due to its ability to interact with biomolecules. Its stability and reactivity also make it suitable for use in materials science, such as in the development of organic electronic devices and polymers.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,339.00
inventory 5g
10-20 days ฿31,500.00
inventory 1g
10-20 days ฿9,000.00
N-(2-Hydroxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of boron-containing compounds. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a precursor for developing bioconjugates and probes in biochemical research, particularly in labeling and imaging applications due to its ability to interact with biomolecules. Its stability and reactivity also make it suitable for use in materials science, such as in the development of organic electronic devices and polymers.
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