(E)-Methyl 3-(3,5-difluoro-4-formylphenyl)acrylate

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Reagent Code: #183595
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CAS Number 1639042-39-9

science Other reagents with same CAS 1639042-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.18 g/mol
Formula C₁₁H₈F₂O₃
badge Registry Numbers
MDL Number MFCD29905622
thermostat Physical Properties
Boiling Point 320.9±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of reactive aldehyde and acrylate functional groups. The α,β-unsaturated ester moiety enables Michael addition reactions, while the aldehyde group allows for condensation or reduction, making it valuable in constructing complex organic molecules. Commonly employed in the development of bioactive compounds, including kinase inhibitors and other therapeutic agents. Its fluorinated aromatic ring enhances metabolic stability and membrane permeability in drug candidates. Also utilized in materials science for designing specialty monomers and functional polymers.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿506.00
inventory 25g
10-20 days ฿35,630.00
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(E)-Methyl 3-(3,5-difluoro-4-formylphenyl)acrylate
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of reactive aldehyde and acrylate functional groups. The α,β-unsaturated ester moiety enables Michael addition reactions, while the aldehyde group allows for condensation or reduction, making it valuable in constructing complex organic molecules. Commonly employed in the development of bioactive compounds, including kinase inhibitors and other therapeutic agents. Its fluorinated aromatic ring

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of reactive aldehyde and acrylate functional groups. The α,β-unsaturated ester moiety enables Michael addition reactions, while the aldehyde group allows for condensation or reduction, making it valuable in constructing complex organic molecules. Commonly employed in the development of bioactive compounds, including kinase inhibitors and other therapeutic agents. Its fluorinated aromatic ring enhances metabolic stability and membrane permeability in drug candidates. Also utilized in materials science for designing specialty monomers and functional polymers.

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