Prop-2-yn-1-yl benzoate

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Reagent Code: #84703
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CAS Number 6750-04-5

science Other reagents with same CAS 6750-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.17 g/mol
Formula C₁₀H₈O₂
badge Registry Numbers
MDL Number MFCD00996341
thermostat Physical Properties
Boiling Point 225-226 °C (lit.)
inventory_2 Storage & Handling
Density 1.106 g/mL at 25 °C (lit.)
Storage 2-8°C

description Product Description

Prop-2-yn-1-yl benzoate is primarily utilized in organic synthesis as a versatile building block. Its structure, featuring both an alkyne and an ester group, makes it valuable for click chemistry reactions, particularly in the formation of triazoles via copper-catalyzed azide-alkyne cycloaddition (CuAAC). This compound is also employed in the development of pharmaceuticals and bioactive molecules, where its alkyne moiety allows for efficient functionalization. Additionally, it serves as a precursor in the synthesis of polymers and advanced materials, contributing to the creation of novel compounds with tailored properties. Its applications extend to research in medicinal chemistry, where it aids in the design and optimization of drug candidates.

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Test Parameter Specification
Appearance Colorless to Faint Yellow Liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,782.00

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Prop-2-yn-1-yl benzoate
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Prop-2-yn-1-yl benzoate is primarily utilized in organic synthesis as a versatile building block. Its structure, featuring both an alkyne and an ester group, makes it valuable for click chemistry reactions, particularly in the formation of triazoles via copper-catalyzed azide-alkyne cycloaddition (CuAAC). This compound is also employed in the development of pharmaceuticals and bioactive molecules, where its alkyne moiety allows for efficient functionalization. Additionally, it serves as a precursor in th

Prop-2-yn-1-yl benzoate is primarily utilized in organic synthesis as a versatile building block. Its structure, featuring both an alkyne and an ester group, makes it valuable for click chemistry reactions, particularly in the formation of triazoles via copper-catalyzed azide-alkyne cycloaddition (CuAAC). This compound is also employed in the development of pharmaceuticals and bioactive molecules, where its alkyne moiety allows for efficient functionalization. Additionally, it serves as a precursor in the synthesis of polymers and advanced materials, contributing to the creation of novel compounds with tailored properties. Its applications extend to research in medicinal chemistry, where it aids in the design and optimization of drug candidates.

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