(E)-5-Phenylpent-2-enoic acid

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Reagent Code: #181101
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CAS Number 55320-96-2

science Other reagents with same CAS 55320-96-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.21 g/mol
Formula C₁₁H₁₂O₂
badge Registry Numbers
MDL Number MFCD18972297
thermostat Physical Properties
Melting Point 105 °C(Solv: ethanol (64-17-5); water (7732-18-5))
Boiling Point 348.9±21.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.101±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its conjugated double bond system makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex carbon skeletons. Commonly employed in the development of anti-inflammatory agents and as a building block in the synthesis of fragrances and flavor compounds due to its aromatic and structural properties. Also utilized in polymer chemistry to modify resin properties by introducing unsaturated functional groups.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,040.00
inventory 1g
10-20 days ฿29,390.00
inventory 100mg
10-20 days ฿6,510.00

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(E)-5-Phenylpent-2-enoic acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its conjugated double bond system makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex carbon skeletons. Commonly employed in the development of anti-inflammatory agents and as a building block in the synthesis of fragrances and flavor compounds due to its aromatic and structural properties. Also utilized in polymer chemistry

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its conjugated double bond system makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex carbon skeletons. Commonly employed in the development of anti-inflammatory agents and as a building block in the synthesis of fragrances and flavor compounds due to its aromatic and structural properties. Also utilized in polymer chemistry to modify resin properties by introducing unsaturated functional groups.

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