2-(Dibenzo[b,d]furan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

≥95%

Reagent Code: #89693
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CAS Number 947770-80-1

science Other reagents with same CAS 947770-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.15 g/mol
Formula C₁₈H₁₉BO₃
badge Registry Numbers
MDL Number MFCD18374015
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used in organic synthesis as a key intermediate for cross-coupling reactions, particularly Suzuki-Miyaura coupling, to construct complex organic molecules. It is valuable in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it essential in the synthesis of biaryl compounds. Also employed in the preparation of organic electronic materials, such as OLEDs and semiconductors, due to its ability to introduce dibenzofuran moieties, which enhance charge transport properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,450.00
inventory 250mg
10-20 days ฿16,200.00

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2-(Dibenzo[b,d]furan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used in organic synthesis as a key intermediate for cross-coupling reactions, particularly Suzuki-Miyaura coupling, to construct complex organic molecules. It is valuable in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it essential in the synthesis of biaryl compounds. Also employed in the preparation of organic electronic materials, such as OLEDs and semiconductors, due to its ability to intr

Used in organic synthesis as a key intermediate for cross-coupling reactions, particularly Suzuki-Miyaura coupling, to construct complex organic molecules. It is valuable in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it essential in the synthesis of biaryl compounds. Also employed in the preparation of organic electronic materials, such as OLEDs and semiconductors, due to its ability to introduce dibenzofuran moieties, which enhance charge transport properties.

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