6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-naphthoic acid

98%

Reagent Code: #131010
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CAS Number 1426082-97-4

science Other reagents with same CAS 1426082-97-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.14 g/mol
Formula C₁₇H₁₉BO₄
badge Registry Numbers
MDL Number MFCD24039389
thermostat Physical Properties
Boiling Point 458.6±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing biaryl structures. Its boronic ester functionality allows it to react with aryl halides under palladium catalysis, enabling the formation of extended aromatic systems. This is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials where naphthalene-based frameworks are required. The carboxylic acid group also provides a convenient handle for further derivatization, such as amide formation or esterification, making it useful in multi-step synthesis and the preparation of functionalized organic molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,140.00
inventory 1g
10-20 days ฿13,690.00

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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-naphthoic acid
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Used primarily in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing biaryl structures. Its boronic ester functionality allows it to react with aryl halides under palladium catalysis, enabling the formation of extended aromatic systems. This is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials where naphthalene-based frameworks are required. The carboxylic acid group also

Used primarily in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing biaryl structures. Its boronic ester functionality allows it to react with aryl halides under palladium catalysis, enabling the formation of extended aromatic systems. This is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials where naphthalene-based frameworks are required. The carboxylic acid group also provides a convenient handle for further derivatization, such as amide formation or esterification, making it useful in multi-step synthesis and the preparation of functionalized organic molecules.

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