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Structure of 215801-31-3
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(E)-3-(1H-Indol-6-yl)acrylic acid features a conjugated enoic acid system linked to the indole scaffold, enabling direct integration into bioactive molecule synthesis. The planar (E)-configured double bond enhances electronic delocalization, while the carboxylic acid group facilitates derivatization. This compound serves as a key building block for indole-based pharmaceuticals and fluorescent probes.
(E)-3-(1H-Indol-6-yl)acrylic acid serves as a versatile building block for synthesizing indole-based bioactive molecules, enabling efficient access to conjugated systems via [4+2] cycloadditions and Pd-catalyzed coupling reactions. Its well-defined (E)-configuration and bench-stable carboxylic acid functionality facilitate straightforward derivatization, purification, and integration into pharmaceutical scaffolds.
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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 : H302-H315-H319-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: