(E)-3-(3,4-Dichlorophenyl)acrylic acid

95%

Reagent Code: #185352
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CAS Number 7312-27-8

science Other reagents with same CAS 7312-27-8

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inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in anticoagulant and anti-inflammatory agents. Its α,β-unsaturated carboxylic acid structure makes it valuable in organic synthesis for forming carbon-carbon bonds via conjugate addition reactions. Also employed in the development of agrochemicals, including herbicides and plant growth regulators, due to its ability to mimic bioactive aromatic compounds. Its halogenated aromatic ring enhances binding affinity in biologically active molecules, making it useful in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿630.00
inventory 5g
10-20 days ฿2,130.00
inventory 25g
10-20 days ฿7,950.00
inventory 100g
10-20 days ฿29,760.00
(E)-3-(3,4-Dichlorophenyl)acrylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in anticoagulant and anti-inflammatory agents. Its α,β-unsaturated carboxylic acid structure makes it valuable in organic synthesis for forming carbon-carbon bonds via conjugate addition reactions. Also employed in the development of agrochemicals, including herbicides and plant growth regulators, due to its ability to mimic bioactive aromatic compounds. Its halogenated aromatic ring enhances binding affinity in biologically act

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in anticoagulant and anti-inflammatory agents. Its α,β-unsaturated carboxylic acid structure makes it valuable in organic synthesis for forming carbon-carbon bonds via conjugate addition reactions. Also employed in the development of agrochemicals, including herbicides and plant growth regulators, due to its ability to mimic bioactive aromatic compounds. Its halogenated aromatic ring enhances binding affinity in biologically active molecules, making it useful in medicinal chemistry for structure-activity relationship (SAR) studies.

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