2-((Trimethylsilyl)ethynyl)benzaldehyde

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Reagent Code: #242412
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CAS Number 77123-58-1

science Other reagents with same CAS 77123-58-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.33 g/mol
Formula C₁₂H₁₄OSi
badge Registry Numbers
MDL Number MFCD04039984
thermostat Physical Properties
Melting Point 48 - 53 ℃
Boiling Point 266.3 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 0.98 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated materials for optoelectronic devices. Its aldehyde group enables condensation reactions, while the trimethylsilyl-protected ethynyl group allows for Sonogashira coupling after deprotection, making it valuable in constructing molecular frameworks for organic semiconductors, sensors, and fluorescent dyes. Commonly employed in the synthesis of polyaryl systems and acetylenic natural product analogs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,200.00
inventory 5g
10-20 days ฿5,690.00

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2-((Trimethylsilyl)ethynyl)benzaldehyde
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Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated materials for optoelectronic devices. Its aldehyde group enables condensation reactions, while the trimethylsilyl-protected ethynyl group allows for Sonogashira coupling after deprotection, making it valuable in constructing molecular frameworks for organic semiconductors, sensors, and fluorescent dyes. Commonly employed in the synthesis of polyaryl systems and acetylenic natural product analogs.
Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated materials for optoelectronic devices. Its aldehyde group enables condensation reactions, while the trimethylsilyl-protected ethynyl group allows for Sonogashira coupling after deprotection, making it valuable in constructing molecular frameworks for organic semiconductors, sensors, and fluorescent dyes. Commonly employed in the synthesis of polyaryl systems and acetylenic natural product analogs.
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