(4-Hydroxyphenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone

≥95%

Reagent Code: #82071
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CAS Number 1208395-99-6

science Other reagents with same CAS 1208395-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.2647 g/mol
Formula C₁₆H₁₂O₃
badge Registry Numbers
MDL Number MFCD28124082
thermostat Physical Properties
Boiling Point 448.1±40.0 °C
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex chemical structures. Its unique structure, featuring both a hydroxyl group and a propargyl ether moiety, makes it a valuable building block in the development of pharmaceuticals and advanced materials. It is often employed in click chemistry reactions, where the alkyne group can participate in cycloaddition reactions to form triazoles, which are important in drug discovery and material science. Additionally, its aromatic ketone functionality allows it to be used in the synthesis of photoactive compounds, which are essential in the development of organic photovoltaics and light-sensitive polymers. Its versatility also extends to the creation of liquid crystal materials, where its rigid aromatic structure contributes to the desired molecular alignment properties.

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Test Parameter Specification
APPEARANCE off-white solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,233.00
inventory 100mg
10-20 days ฿3,096.00
inventory 1g
10-20 days ฿7,227.00

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(4-Hydroxyphenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone
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This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex chemical structures. Its unique structure, featuring both a hydroxyl group and a propargyl ether moiety, makes it a valuable building block in the development of pharmaceuticals and advanced materials. It is often employed in click chemistry reactions, where the alkyne group can participate in cycloaddition reactions to form triazoles, which are important in drug discov

This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex chemical structures. Its unique structure, featuring both a hydroxyl group and a propargyl ether moiety, makes it a valuable building block in the development of pharmaceuticals and advanced materials. It is often employed in click chemistry reactions, where the alkyne group can participate in cycloaddition reactions to form triazoles, which are important in drug discovery and material science. Additionally, its aromatic ketone functionality allows it to be used in the synthesis of photoactive compounds, which are essential in the development of organic photovoltaics and light-sensitive polymers. Its versatility also extends to the creation of liquid crystal materials, where its rigid aromatic structure contributes to the desired molecular alignment properties.

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