6-Methoxy-2-naphthaleneboronic acid

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Reagent Code: #90965
label
Alias 6-methoxy-2-naphthylboronic acid
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CAS Number 156641-98-4

science Other reagents with same CAS 156641-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.01 g/mol
Formula C₁₁H₁₁BO₃
badge Registry Numbers
MDL Number MFCD03093087
thermostat Physical Properties
Melting Point >295 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) like Naproxen. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for creating complex organic molecules. Additionally, it is employed in the development of advanced materials and organic electronics due to its ability to facilitate precise molecular construction. Its boronic acid group makes it valuable in sensors and diagnostic applications, particularly in detecting sugars and other biologically relevant molecules.

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Test Parameter Specification
Purity 96.5-100
Appearance White to off-white solid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿1,320.00
inventory 25g
10-20 days ฿4,520.00
inventory 100g
10-20 days ฿16,000.00

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6-Methoxy-2-naphthaleneboronic acid
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Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) like Naproxen. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for creating complex organic molecules. Additionally, it is employed in the development of advanced materials and organic electronics due to its ability to facilitate precise molecular construction. Its boronic a
Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) like Naproxen. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for creating complex organic molecules. Additionally, it is employed in the development of advanced materials and organic electronics due to its ability to facilitate precise molecular construction. Its boronic acid group makes it valuable in sensors and diagnostic applications, particularly in detecting sugars and other biologically relevant molecules.
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