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Structure of 50562-79-3
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1-(4-Tolylsulfonyl)indole-3-carboxaldehyde features a reactive aldehyde group flanked by an electron-deficient indole core and a bulky tolylsulfonyl substituent. This combination enhances stability while enabling selective coupling reactions in synthetic medicinal chemistry. The molecule serves as a key intermediate for constructing complex heterocyclic scaffolds under mild conditions.
1-(4-Tolylsulfonyl)indole-3-carboxaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to indole-based scaffolds through electrophilic substitution and coupling reactions. The aldehyde functionality facilitates direct functionalization or conjugation, while the 4-tolylsulfonyl group provides excellent stability and orthogonal reactivity. This compound is particularly useful in medicinal chemistry campaigns requiring robust, bench-stable intermediates for API 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: