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Structure of 25522-33-2
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trans-Isoferulic acid features a stable trans-configuration at the C=C bond, enhancing its thermal and oxidative robustness. This configuration imparts distinct electronic properties ideal for conjugated systems. The molecule bears a para-hydroxy cinnamate scaffold with a methyl-substituted aromatic ring, enabling predictable reactivity in coupling reactions. Its bench-stable nature simplifies handling under standard conditions.
trans-Isoferulic acid serves as a valuable building block in the synthesis of bioactive heterocycles and pharmaceutical intermediates, leveraging its conjugated diene system and carboxylic acid functionality. Its bench-stable nature and compatibility with standard coupling reactions enable efficient derivatization for medicinal chemistry applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: