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Structure of 60011-16-7
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(S)-S-tert-Butyl 2-methylpropane-2-sulfinothioate features a chiral sulfinothioate moiety with enhanced stability and excellent solubility in organic media. This bench-stable reagent enables stereoselective sulfur transfer reactions under mild conditions, serving as a robust precursor in asymmetric synthesis.
(S)-S-tert-Butyl 2-methylpropane-2-sulfinothioate serves as a chiral sulfine-based building block, enabling stereoselective sulfur-transfer reactions in synthetic sequences. Its tert-butyl thioether functionality offers enhanced bench stability and facilitates straightforward purification. The molecule functions effectively in transition-metal-catalyzed couplings and acts as a masked sulfenylating agent, supporting the construction of complex thioether-containing architectures with high configurational integrity.
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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: