2-(3-Decylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #130916
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CAS Number 1403967-25-8

science Other reagents with same CAS 1403967-25-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.37 g/mol
Formula C₂₀H₃₅BO₂S
thermostat Physical Properties
Boiling Point 441.0±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.97±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of conjugated organic materials for applications in organic semiconductors, photovoltaics, and light-emitting diodes (OLEDs). The boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in the preparation of complex π-conjugated systems. Its decyl chain enhances solubility in organic solvents, which supports solution-processable electronic device fabrication. Commonly employed in research and development of organic electronic materials and pharmaceuticals requiring tailored aromatic structures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,500.00

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2-(3-Decylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of conjugated organic materials for applications in organic semiconductors, photovoltaics, and light-emitting diodes (OLEDs). The boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in the preparation of complex π-conjugated systems. Its decyl chain enhances solubility in organic solvents, which supports solution-processable electronic device fabricat

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of conjugated organic materials for applications in organic semiconductors, photovoltaics, and light-emitting diodes (OLEDs). The boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in the preparation of complex π-conjugated systems. Its decyl chain enhances solubility in organic solvents, which supports solution-processable electronic device fabrication. Commonly employed in research and development of organic electronic materials and pharmaceuticals requiring tailored aromatic structures.

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