(2E)-3-Methyl-4-oxo-4-phenyl-2-butenoic acid

≥95%

Reagent Code: #180894
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CAS Number 35504-92-8

science Other reagents with same CAS 35504-92-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.1953 g/mol
Formula C₁₁H₁₀O₃
thermostat Physical Properties
Melting Point 101-102 °C
Boiling Point 343.4±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.199±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its α,β-unsaturated carbonyl structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Commonly employed in the development of anti-inflammatory and antimicrobial agents due to its ability to act as a building block for heterocyclic compounds. Also utilized in research settings for the synthesis of cinnamic acid derivatives and related bioactive molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿24,000.00
inventory 1g
10-20 days ฿72,000.00

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(2E)-3-Methyl-4-oxo-4-phenyl-2-butenoic acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its α,β-unsaturated carbonyl structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Commonly employed in the development of anti-inflammatory and antimicrobial agents due to its ability to act as a building block for heterocyclic compounds. Also utilized in research settings for the synthesis of c

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its α,β-unsaturated carbonyl structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Commonly employed in the development of anti-inflammatory and antimicrobial agents due to its ability to act as a building block for heterocyclic compounds. Also utilized in research settings for the synthesis of cinnamic acid derivatives and related bioactive molecules.

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