4,4,5,5-Tetramethyl-2-(selenophen-2-yl)-1,3,2-dioxaborolane

≥95%

Reagent Code: #45826
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CAS Number 1338368-18-5

science Other reagents with same CAS 1338368-18-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.99 g/mol
Formula C₁₀H₁₅BO₂Se
badge Registry Numbers
MDL Number MFCD28969360
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for introducing selenophene rings into more complex organic molecules, which are valuable in the development of organic semiconductors and optoelectronic materials. Its boronate ester group facilitates efficient coupling with aryl halides, enabling the construction of conjugated systems. These systems are essential in the production of materials for organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and other electronic devices. Additionally, its stability and reactivity make it a useful reagent in medicinal chemistry for designing novel drug candidates.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity (%) 95.0-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,365.00
inventory 250mg
10-20 days ฿8,730.00

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4,4,5,5-Tetramethyl-2-(selenophen-2-yl)-1,3,2-dioxaborolane
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for introducing selenophene rings into more complex organic molecules, which are valuable in the development of organic semiconductors and optoelectronic materials. Its boronate ester group facilitates efficient coupling with aryl halides, enabling the construction of conjugated systems. These systems are essential in the production of materia

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for introducing selenophene rings into more complex organic molecules, which are valuable in the development of organic semiconductors and optoelectronic materials. Its boronate ester group facilitates efficient coupling with aryl halides, enabling the construction of conjugated systems. These systems are essential in the production of materials for organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and other electronic devices. Additionally, its stability and reactivity make it a useful reagent in medicinal chemistry for designing novel drug candidates.

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