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*For research and further manufacturing use only, not for direct human use.
Structure of 670-98-4
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Methyl benzenesulfinate delivers a stable, bench-ready sulfination reagent with enhanced solubility in organic media. The methylthio group facilitates efficient coupling under mild conditions, enabling direct functionalization of heteroatom nucleophiles. This reagent integrates seamlessly into synthetic workflows requiring selective sulfur transfer without the need for stoichiometric metal catalysts.
Methyl benzenesulfinate serves as a versatile sulfination reagent, enabling efficient introduction of sulfonyl groups in synthetic workflows. Its bench-stable nature and compatibility with diverse functional groups facilitate reliable transformations in the construction of sulfonamide derivatives and heterocyclic scaffolds commonly encountered in medicinal chemistry.
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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: