1-Iodo-2-(trimethylsilyl)acetylene

90%

Reagent Code: #199145
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Alias 1-Iodine-2-trisilylacetylene
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CAS Number 18163-47-8

science Other reagents with same CAS 18163-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.11 g/mol
Formula C₅H₉ISi
badge Registry Numbers
MDL Number MFCD00274201
thermostat Physical Properties
Boiling Point 130 °C(lit.)
inventory_2 Storage & Handling
Density 1.46 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used in organic synthesis as a versatile building block for carbon-carbon bond formation, particularly in Sonogashira and other palladium-catalyzed coupling reactions. Enables the introduction of trimethylsilylacetylene groups into complex molecules, facilitating the preparation of conjugated enynes and arylalkynes for materials science and pharmaceutical research. The iodo group acts as a reactive handle, while the trimethylsilyl group stabilizes the alkyne and can be removed selectively to generate terminal alkynes. Commonly employed in the synthesis of natural products, molecular electronics, and functional polymers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿1,090.00
inventory 25g
10-20 days ฿5,340.00
1-Iodo-2-(trimethylsilyl)acetylene
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Used in organic synthesis as a versatile building block for carbon-carbon bond formation, particularly in Sonogashira and other palladium-catalyzed coupling reactions. Enables the introduction of trimethylsilylacetylene groups into complex molecules, facilitating the preparation of conjugated enynes and arylalkynes for materials science and pharmaceutical research. The iodo group acts as a reactive handle, while the trimethylsilyl group stabilizes the alkyne and can be removed selectively to generate ter

Used in organic synthesis as a versatile building block for carbon-carbon bond formation, particularly in Sonogashira and other palladium-catalyzed coupling reactions. Enables the introduction of trimethylsilylacetylene groups into complex molecules, facilitating the preparation of conjugated enynes and arylalkynes for materials science and pharmaceutical research. The iodo group acts as a reactive handle, while the trimethylsilyl group stabilizes the alkyne and can be removed selectively to generate terminal alkynes. Commonly employed in the synthesis of natural products, molecular electronics, and functional polymers.

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