(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid

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Reagent Code: #90281
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CAS Number 380430-62-6

science Other reagents with same CAS 380430-62-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.0592 g/mol
Formula C₁₄H₁₂BNO₆
badge Registry Numbers
MDL Number MFCD03411934
thermostat Physical Properties
Melting Point 140-148 ℃
Boiling Point 537.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.40±0.1 g/cm3
Storage 2-8°C

description Product Description

(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key intermediate for constructing complex aromatic compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are essential in pharmaceuticals and agrochemicals. Additionally, the benzyloxycarbonyl protecting group enhances its stability during synthetic processes, making it a valuable reagent in multi-step organic transformations. The nitro group further allows for subsequent functionalization, expanding its utility in the development of advanced materials and bioactive molecules.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿27,792.00
inventory 1g
10-20 days ฿8,802.00

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(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid
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(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key intermediate for constructing complex aromatic compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are essential in pharmaceuticals and agrochemicals. Additionally, the benzyloxycarbonyl protecting group enhances its stability duri

(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key intermediate for constructing complex aromatic compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are essential in pharmaceuticals and agrochemicals. Additionally, the benzyloxycarbonyl protecting group enhances its stability during synthetic processes, making it a valuable reagent in multi-step organic transformations. The nitro group further allows for subsequent functionalization, expanding its utility in the development of advanced materials and bioactive molecules.

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