[4-(Prop-2-yn-1-yl)phenyl]methanol

95%

Reagent Code: #227186
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CAS Number 51176-48-8

science Other reagents with same CAS 51176-48-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.19 g/mol
Formula C₁₀H₁₀O
badge Registry Numbers
MDL Number MFCD26398694
inventory_2 Storage & Handling
Storage -20°C, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Its alkyne group enables click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in bioconjugation, drug discovery, and polymer chemistry. The hydroxyl group allows further functionalization, such as esterification or ether formation, enabling its incorporation into more complex molecular architectures. Commonly employed in the development of probes, sensors, and functionalized molecules for research in medicinal and materials chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,230.00
inventory 100mg
10-20 days ฿6,846.00
inventory 250mg
10-20 days ฿11,790.00
[4-(Prop-2-yn-1-yl)phenyl]methanol
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Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Its alkyne group enables click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in bioconjugation, drug discovery, and polymer chemistry. The hydroxyl group allows further functionalization, such as esterification or ether formation, enabling its incorporation into more complex molecular architectures. Commonly employed in the development of probes, sensors,

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Its alkyne group enables click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in bioconjugation, drug discovery, and polymer chemistry. The hydroxyl group allows further functionalization, such as esterification or ether formation, enabling its incorporation into more complex molecular architectures. Commonly employed in the development of probes, sensors, and functionalized molecules for research in medicinal and materials chemistry.

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