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Structure of 356068-93-4
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This (Z)-configured pyrrole derivative features a fluorinated oxindole moiety linked via a methylidene bridge, delivering enhanced stability and targeted reactivity. The electron-deficient pyrrole core, combined with sterically hindered methyl groups, enables selective conjugation in synthetic and medicinal chemistry applications.
(Z)-5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid serves as a versatile building block for the synthesis of fluorinated indoline-containing heterocycles. Its conjugated enone system enables efficient Michael additions and cycloaddition reactions, while the carboxylic acid group facilitates direct derivatization or salt formation. The molecule exhibits bench stability and compatibility with standard purification methods, making it suitable for iterative synthetic workflows in medicinal chemistry and process development.
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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 : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: