N-(4-Hydroxyphenyl)acrylamide

98%, contains MEHQ as stabilizer

Reagent Code: #215671
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CAS Number 34443-04-4

science Other reagents with same CAS 34443-04-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.17 g/mol
Formula C₉H₉NO₂
badge Registry Numbers
MDL Number MFCD01673905
thermostat Physical Properties
Boiling Point 385.9±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.231±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used in the synthesis of pharmaceuticals and bioactive compounds due to its ability to act as a building block for more complex molecules. Its phenolic hydroxyl and amide functional groups allow for easy modification, making it valuable in medicinal chemistry. Commonly employed in the development of kinase inhibitors and anti-inflammatory agents. Also utilized in polymer chemistry to create functionalized hydrogels and responsive materials, where the compound contributes to improved biocompatibility and targeted drug delivery systems. Its structure supports conjugation with biomolecules, enabling applications in bioconjugation and labeling techniques.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,200.00
inventory 1g
10-20 days ฿6,200.00
inventory 5g
10-20 days ฿22,300.00

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N-(4-Hydroxyphenyl)acrylamide
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Used in the synthesis of pharmaceuticals and bioactive compounds due to its ability to act as a building block for more complex molecules. Its phenolic hydroxyl and amide functional groups allow for easy modification, making it valuable in medicinal chemistry. Commonly employed in the development of kinase inhibitors and anti-inflammatory agents. Also utilized in polymer chemistry to create functionalized hydrogels and responsive materials, where the compound contributes to improved biocompatibility and

Used in the synthesis of pharmaceuticals and bioactive compounds due to its ability to act as a building block for more complex molecules. Its phenolic hydroxyl and amide functional groups allow for easy modification, making it valuable in medicinal chemistry. Commonly employed in the development of kinase inhibitors and anti-inflammatory agents. Also utilized in polymer chemistry to create functionalized hydrogels and responsive materials, where the compound contributes to improved biocompatibility and targeted drug delivery systems. Its structure supports conjugation with biomolecules, enabling applications in bioconjugation and labeling techniques.

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