3-(Trimethylsilyl)propargyl alcohol

95%

Reagent Code: #240467
label
Alias 3-Trisilyl-2-propyne-1-ol
fingerprint
CAS Number 5272-36-6

science Other reagents with same CAS 5272-36-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.24 g/mol
Formula C₆H₁₂OSi
badge Registry Numbers
EC Number 226-094-5
MDL Number MFCD00002913
thermostat Physical Properties
Boiling Point 76 °C11 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.865 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of silane-based coupling agents and functionalized polymers. Its alkyne and hydroxyl groups allow for dual reactivity, enabling use in click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), to build complex molecules for pharmaceuticals and agrochemicals. Commonly employed in the synthesis of silyl-protected propargyl derivatives for semiconductor manufacturing and in the development of specialty coatings with enhanced thermal and oxidative stability. Also finds application in the creation of fluorescent probes and bioconjugates due to its ability to undergo selective transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿690.00
inventory 25ml
10-20 days ฿2,500.00
inventory 100ml
10-20 days ฿8,780.00
3-(Trimethylsilyl)propargyl alcohol
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Used as a key intermediate in organic synthesis, particularly in the preparation of silane-based coupling agents and functionalized polymers. Its alkyne and hydroxyl groups allow for dual reactivity, enabling use in click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), to build complex molecules for pharmaceuticals and agrochemicals. Commonly employed in the synthesis of silyl-protected propargyl derivatives for semiconductor manufacturing and in the development of specialty coati

Used as a key intermediate in organic synthesis, particularly in the preparation of silane-based coupling agents and functionalized polymers. Its alkyne and hydroxyl groups allow for dual reactivity, enabling use in click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), to build complex molecules for pharmaceuticals and agrochemicals. Commonly employed in the synthesis of silyl-protected propargyl derivatives for semiconductor manufacturing and in the development of specialty coatings with enhanced thermal and oxidative stability. Also finds application in the creation of fluorescent probes and bioconjugates due to its ability to undergo selective transformations.

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