But-3-yn-1-yl methanesulfonate

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Reagent Code: #84182
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CAS Number 72486-09-0

science Other reagents with same CAS 72486-09-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 148.18 g/mol
Formula C₅H₈O₃S
badge Registry Numbers
MDL Number MFCD12912983
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

But-3-yn-1-yl methanesulfonate is primarily used as a reactive intermediate in organic synthesis. Its alkyne functional group makes it valuable for click chemistry reactions, particularly in the formation of triazoles through copper-catalyzed azide-alkyne cycloaddition (CuAAC). This compound is also employed in the modification of biomolecules, such as peptides and proteins, enabling the attachment of functional groups or labels for biochemical studies. Additionally, it serves as a building block in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, due to its ability to introduce alkyne moieties into target structures. Its methanesulfonate group further enhances its reactivity, making it a versatile reagent in various chemical transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,600.00
inventory 250mg
10-20 days ฿7,200.00
inventory 1g
10-20 days ฿14,400.00

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But-3-yn-1-yl methanesulfonate
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But-3-yn-1-yl methanesulfonate is primarily used as a reactive intermediate in organic synthesis. Its alkyne functional group makes it valuable for click chemistry reactions, particularly in the formation of triazoles through copper-catalyzed azide-alkyne cycloaddition (CuAAC). This compound is also employed in the modification of biomolecules, such as peptides and proteins, enabling the attachment of functional groups or labels for biochemical studies. Additionally, it serves as a building block in the

But-3-yn-1-yl methanesulfonate is primarily used as a reactive intermediate in organic synthesis. Its alkyne functional group makes it valuable for click chemistry reactions, particularly in the formation of triazoles through copper-catalyzed azide-alkyne cycloaddition (CuAAC). This compound is also employed in the modification of biomolecules, such as peptides and proteins, enabling the attachment of functional groups or labels for biochemical studies. Additionally, it serves as a building block in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, due to its ability to introduce alkyne moieties into target structures. Its methanesulfonate group further enhances its reactivity, making it a versatile reagent in various chemical transformations.

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