4,4,5,5-Tetramethyl-2-(naphthalen-1-ylmethyl)-1,3,2-dioxaborolane

≥95%

Reagent Code: #90303
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CAS Number 475250-57-8

science Other reagents with same CAS 475250-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.16 g/mol
Formula C₁₇H₂₁BO₂
badge Registry Numbers
MDL Number MFCD22419278
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, specifically a benzylic boronic ester derived from 1-naphthylmethyl, enabling the formation of carbon-carbon bonds by coupling the 1-naphthylmethyl group with aryl or vinyl halides. This process is widely applied in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable tool in the development of new compounds, especially in medicinal chemistry for drug discovery and development. Additionally, it is used in the preparation of functionalized polymers and materials for electronic applications.

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Test Parameter Specification
Appearance white to off-white solid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,854.00

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4,4,5,5-Tetramethyl-2-(naphthalen-1-ylmethyl)-1,3,2-dioxaborolane
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, specifically a benzylic boronic ester derived from 1-naphthylmethyl, enabling the formation of carbon-carbon bonds by coupling the 1-naphthylmethyl group with aryl or vinyl halides. This process is widely applied in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity m

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, specifically a benzylic boronic ester derived from 1-naphthylmethyl, enabling the formation of carbon-carbon bonds by coupling the 1-naphthylmethyl group with aryl or vinyl halides. This process is widely applied in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable tool in the development of new compounds, especially in medicinal chemistry for drug discovery and development. Additionally, it is used in the preparation of functionalized polymers and materials for electronic applications.

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