4-nitrophenylboronic acid

≥95%

Reagent Code: #90708
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CAS Number 24067-17-2

science Other reagents with same CAS 24067-17-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.93 g/mol
Formula C₆H₆BNO₄
badge Registry Numbers
MDL Number MFCD00161360
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds in pharmaceutical and material science research. It acts as a boronic acid derivative in organic synthesis, enabling the formation of carbon-carbon bonds. Additionally, it serves as a building block in the development of sensors for detecting sugars and other diol-containing molecules due to its ability to form reversible covalent bonds with diols. It is also employed in the preparation of advanced materials, such as polymers and metal-organic frameworks, for applications in catalysis and molecular recognition.

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Test Parameter Specification
Purity 95-100%
Appearance White to brown crystalline powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿600.00
inventory 5g
10-20 days ฿2,950.00
inventory 25g
10-20 days ฿13,590.00

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4-nitrophenylboronic acid
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds in pharmaceutical and material science research. It acts as a boronic acid derivative in organic synthesis, enabling the formation of carbon-carbon bonds. Additionally, it serves as a building block in the development of sensors for detecting sugars and other diol-containing molecules due to its ability to form reversible covalent bonds with diols. It is also employed in the preparation of adv

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds in pharmaceutical and material science research. It acts as a boronic acid derivative in organic synthesis, enabling the formation of carbon-carbon bonds. Additionally, it serves as a building block in the development of sensors for detecting sugars and other diol-containing molecules due to its ability to form reversible covalent bonds with diols. It is also employed in the preparation of advanced materials, such as polymers and metal-organic frameworks, for applications in catalysis and molecular recognition.

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