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Structure of 247923-41-7
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This sulfonamide features a chiral aminoethyl scaffold paired with a sterically shielded trisisopropylbenzene group, delivering enhanced stability and solubility in organic media. The bulky isopropyl substituents minimize aggregation while the amine functionality enables facile derivatization. Designed for use in asymmetric synthesis and catalyst design, this compound combines steric protection with tunable reactivity.
N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-2,4,6-trisisopropylbenzenesulfonamide serves as a sterically encumbered sulfonamide building block for asymmetric synthesis. The (1S,2S)-configured aminoethyl moiety enables stereoselective transformations, while the trisisopropylphenyl group imparts exceptional steric shielding and bench stability. This scaffold facilitates efficient amide bond formation and functions as a protected amine in multi-step sequences, offering high functional group tolerance and ease of purification in complex molecule assembly.
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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: