1,3,2-Dioxaborolane, 2-(9,9-Dimethyl-9H-Fluoren-2-YL)-4,4,5,5-Tetramethyl
≥98%
Reagent
Code: #91199
CAS Number
569343-09-5
blur_circular Chemical Specifications
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Molecular Information
Weight
320.24 g/mol
Formula
C₂₁H₂₅BO₂
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Storage & Handling
Storage
room temperature, dry
description Product Description
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its ability to enhance charge transport properties. Its stability and reactivity also make it a preferred choice in polymer chemistry for creating functionalized polymers with tailored properties.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White - almost white crystal - powder |
Purity | 97.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
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1,3,2-Dioxaborolane, 2-(9,9-Dimethyl-9H-Fluoren-2-YL)-4,4,5,5-Tetramethyl
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its ability to enhance charge transport properties. Its stability and reactivity also make it a preferred choice in polymer chemistry for creating functionalized polymers with tailored properties.
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