dimethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-dicarboxylate

≥98%

Reagent Code: #89950
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CAS Number 944392-68-1

science Other reagents with same CAS 944392-68-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.15 g/mol
Formula C₁₆H₂₁BO₆
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing complex aromatic structures, which are essential in the development of pharmaceuticals, agrochemicals, and organic materials. The compound’s stability and reactivity allow for precise and efficient bond formation, enabling the synthesis of biologically active molecules and advanced polymers. Additionally, it serves as a key building block in the preparation of organic electronic materials, contributing to the development of optoelectronic devices like OLEDs and organic solar cells.

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Test Parameter Specification
Appearance White to off-white Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,970.00
inventory 200mg
10-20 days ฿1,060.00
inventory 1g
10-20 days ฿1,930.00

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dimethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-dicarboxylate
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing complex aromatic structures, which are essential in the development of pharmaceuticals, agrochemicals, and organic materials. The compound’s stability and reactivity allow for precise and efficient bond formation, enabling the synthesis of biologically active molecules and advanced polymers. Additionally, it serves as a key building block in the preparation of organic electronic materials, contributing to the development of optoelectronic devices like OLEDs and organic solar cells.
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