Propargyl p-toluenesulfonate

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Reagent Code: #224813
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Alias Propynyl p-toluenesulfonate
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CAS Number 6165-76-0

science Other reagents with same CAS 6165-76-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.25 g/mol
Formula C₁₀H₁₀O₃S
badge Registry Numbers
MDL Number MFCD01462194
thermostat Physical Properties
Boiling Point 117-121°C 0,3mm
inventory_2 Storage & Handling
Density 1.215 g/mL at 20 °C(lit.)
Storage 2~8°C

description Product Description

Used as a versatile alkylating agent in organic synthesis, particularly in the preparation of propargylated derivatives for pharmaceuticals and fine chemicals. Its reactivity makes it valuable in introducing propargyl groups into nucleophilic substrates, enabling subsequent transformations such as click chemistry via copper-catalyzed azide-alkyne cycloaddition (CuAAC). Commonly employed in the synthesis of complex molecules including natural products and bioactive compounds, where the alkyne functionality serves as a chemical handle for further modification. Also utilized in polymer chemistry to introduce functional groups that enhance material properties or enable crosslinking.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1ml
10-20 days ฿650.00
5ml
10-20 days ฿1,420.00
25ml
10-20 days ฿5,350.00
100ml
10-20 days ฿19,780.00
Propargyl p-toluenesulfonate
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Used as a versatile alkylating agent in organic synthesis, particularly in the preparation of propargylated derivatives for pharmaceuticals and fine chemicals. Its reactivity makes it valuable in introducing propargyl groups into nucleophilic substrates, enabling subsequent transformations such as click chemistry via copper-catalyzed azide-alkyne cycloaddition (CuAAC). Commonly employed in the synthesis of complex molecules including natural products and bioactive compounds, where the alkyne functionalit

Used as a versatile alkylating agent in organic synthesis, particularly in the preparation of propargylated derivatives for pharmaceuticals and fine chemicals. Its reactivity makes it valuable in introducing propargyl groups into nucleophilic substrates, enabling subsequent transformations such as click chemistry via copper-catalyzed azide-alkyne cycloaddition (CuAAC). Commonly employed in the synthesis of complex molecules including natural products and bioactive compounds, where the alkyne functionality serves as a chemical handle for further modification. Also utilized in polymer chemistry to introduce functional groups that enhance material properties or enable crosslinking.

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