2-(benzo[b]thiophen-2-yl)-5,5-dimethyl-1,3,2-dioxaborolane

98%

Reagent Code: #148012
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CAS Number 568572-21-4

science Other reagents with same CAS 568572-21-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.133 g/mol
Formula C₁₃H₁₅BO₂S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of biaryl and heterobiaryl compounds, which are common structural motifs in pharmaceuticals and agrochemicals. Its benzo[b]thiophene moiety is valuable for constructing conjugated systems in materials science, including organic semiconductors and optoelectronic materials. The presence of the dioxaborolane group enhances stability and reactivity under palladium-catalyzed conditions, making it suitable for late-stage functionalization in drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿880.00
inventory 1g
10-20 days ฿2,680.00
inventory 5g
10-20 days ฿10,870.00

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2-(benzo[b]thiophen-2-yl)-5,5-dimethyl-1,3,2-dioxaborolane
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Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of biaryl and heterobiaryl compounds, which are common structural motifs in pharmaceuticals and agrochemicals. Its benzo[b]thiophene moiety is valuable for constructing conjugated systems in materials science, including organic semiconductors and optoelectronic materials. The presence of the dioxaborolane group enhances stability and reactivity under palladium-catalyzed conditions, making it suitable for late-stage functionalization in drug discovery.
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