8-((Trimethylsilyl)ethynyl)isoquinoline

95%

Reagent Code: #244586
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CAS Number 1823440-48-7

science Other reagents with same CAS 1823440-48-7

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Weight 225.36 g/mol
Formula C₁₄H₁₅NSi
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MDL Number MFCD28346927
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic light-emitting diodes (OLEDs) as an intermediate for electron-transport materials due to its conjugated structure and thermal stability. Its silyl-protected alkyne group allows for efficient cross-coupling reactions in the synthesis of complex isoquinoline-based emitters. Also employed in the development of fluorescent sensors and bioimaging probes, where the rigid isoquinoline core enhances photoluminescence quantum yield. The compound’s lipophilicity improves membrane permeability in cellular imaging applications. Additionally, it serves as a building block in click chemistry for constructing conjugated polymers used in optoelectronic devices.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿70,630.00
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8-((Trimethylsilyl)ethynyl)isoquinoline
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Used in organic light-emitting diodes (OLEDs) as an intermediate for electron-transport materials due to its conjugated structure and thermal stability. Its silyl-protected alkyne group allows for efficient cross-coupling reactions in the synthesis of complex isoquinoline-based emitters. Also employed in the development of fluorescent sensors and bioimaging probes, where the rigid isoquinoline core enhances photoluminescence quantum yield. The compound’s lipophilicity improves membrane permeability in ce

Used in organic light-emitting diodes (OLEDs) as an intermediate for electron-transport materials due to its conjugated structure and thermal stability. Its silyl-protected alkyne group allows for efficient cross-coupling reactions in the synthesis of complex isoquinoline-based emitters. Also employed in the development of fluorescent sensors and bioimaging probes, where the rigid isoquinoline core enhances photoluminescence quantum yield. The compound’s lipophilicity improves membrane permeability in cellular imaging applications. Additionally, it serves as a building block in click chemistry for constructing conjugated polymers used in optoelectronic devices.

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