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Structure of 881677-11-8
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This pyrrole-based aldehyde features a fluorinated aryl group and a pyridine sulfonamide moiety, delivering enhanced electronic modulation and solubility. The para-fluorophenyl substitution improves metabolic stability, while the sulfonylpyridine handle enables efficient conjugation in synthetic workflows. Bench-stable under standard conditions, this compound integrates readily into complex molecular architectures.
5-(2-Fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling the construction of heterocyclic scaffolds via standard coupling and functional group transformation protocols. The pyrrole core exhibits stability under routine reaction conditions, while the aldehyde functionality facilitates efficient derivatization through reductive amination, cyanohydrin formation, or condensation reactions. The ortho-fluorophenyl and pyridinylsulfonyl groups provide enhanced metabolic stability and tunable solubility, supporting downstream optimization in API development workflows.
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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: