4-Methylamino-3-nitrophenylboronic acid,pinacol ester

98%

Reagent Code: #90699
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CAS Number 956821-93-5

science Other reagents with same CAS 956821-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.11 g/mol
Formula C₁₃H₁₉BN₂O₄
badge Registry Numbers
MDL Number MFCD12026089
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, essential in constructing pharmaceuticals and advanced materials. Additionally, its boronic ester group makes it useful in the development of sensors and diagnostic agents, especially for detecting sugars and other biologically relevant molecules. Its stability and reactivity also make it a candidate for use in polymer chemistry and material science, where it can be incorporated into polymers to modify their properties or create new functional materials.

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Test Parameter Specification
Appearance Yellow to Orange to Brown Powder
Purity (%) 94.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,349.00
inventory 1g
10-20 days ฿9,000.00

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4-Methylamino-3-nitrophenylboronic acid,pinacol ester
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, essential in constructing pharmaceuticals and advanced materials. Additionally, its boronic ester group makes it useful in the development of sensors and diagnostic agents, especially for detecting sugars and other biologically relevant molecules. Its

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, essential in constructing pharmaceuticals and advanced materials. Additionally, its boronic ester group makes it useful in the development of sensors and diagnostic agents, especially for detecting sugars and other biologically relevant molecules. Its stability and reactivity also make it a candidate for use in polymer chemistry and material science, where it can be incorporated into polymers to modify their properties or create new functional materials.

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