3-Hydroxy-5-nitrophenylboronic acid

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Reagent Code: #90267
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CAS Number 737001-07-9

science Other reagents with same CAS 737001-07-9

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scatter_plot Molecular Information
Weight 182.93 g/mol
Formula C₆H₆BNO₅
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MDL Number MFCD05664060
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used in organic synthesis as a reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. It is also employed in the development of sensors for detecting sugars and other diol-containing compounds due to its boronic acid group, which forms reversible covalent bonds with cis-diols. Additionally, it finds application in the preparation of pharmaceutical intermediates and in materials science for creating functionalized polymers and coatings.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿81,540.00

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3-Hydroxy-5-nitrophenylboronic acid
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Used in organic synthesis as a reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. It is also employed in the development of sensors for detecting sugars and other diol-containing compounds due to its boronic acid group, which forms reversible covalent bonds with cis-diols. Additionally, it finds application in the preparation of pharmaceutical intermediates and in materials science for creating functionalized

Used in organic synthesis as a reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. It is also employed in the development of sensors for detecting sugars and other diol-containing compounds due to its boronic acid group, which forms reversible covalent bonds with cis-diols. Additionally, it finds application in the preparation of pharmaceutical intermediates and in materials science for creating functionalized polymers and coatings.

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