tert-Butyldimethyl(pent-4-yn-1-yloxy)silane

98%

Reagent Code: #153440
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CAS Number 61362-77-4

science Other reagents with same CAS 61362-77-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.38 g/mol
Formula C₁₁H₂₂OSi
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

tert-Butyldimethyl(pent-4-yn-1-yloxy)silane is the tert-butyldimethylsilyl (TBDMS) protected form of pent-4-yn-1-ol, serving as a versatile building block in organic synthesis. The TBDMS group protects the hydroxyl functionality, allowing selective manipulation of the terminal alkyne or other reactive sites under various reaction conditions. It offers stability and steric hindrance to minimize side reactions, with deprotection achievable selectively using fluoride ions or acidic conditions. This compound is widely used in multi-step syntheses of complex molecules, including natural products, pharmaceuticals, agrochemical intermediates, and specialty materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿530.00
1g
10-20 days ฿1,480.00
tert-Butyldimethyl(pent-4-yn-1-yloxy)silane
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tert-Butyldimethyl(pent-4-yn-1-yloxy)silane is the tert-butyldimethylsilyl (TBDMS) protected form of pent-4-yn-1-ol, serving as a versatile building block in organic synthesis. The TBDMS group protects the hydroxyl functionality, allowing selective manipulation of the terminal alkyne or other reactive sites under various reaction conditions. It offers stability and steric hindrance to minimize side reactions, with deprotection achievable selectively using fluoride ions or acidic conditions. This compound

tert-Butyldimethyl(pent-4-yn-1-yloxy)silane is the tert-butyldimethylsilyl (TBDMS) protected form of pent-4-yn-1-ol, serving as a versatile building block in organic synthesis. The TBDMS group protects the hydroxyl functionality, allowing selective manipulation of the terminal alkyne or other reactive sites under various reaction conditions. It offers stability and steric hindrance to minimize side reactions, with deprotection achievable selectively using fluoride ions or acidic conditions. This compound is widely used in multi-step syntheses of complex molecules, including natural products, pharmaceuticals, agrochemical intermediates, and specialty materials.

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