Lot numbers can be found on the outside label of a product:
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Structure of 640-60-8
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Phenyl p-toluenesulfonate serves as a robust arylating agent in nucleophilic substitution reactions. This bench-stable, moisture-tolerant reagent facilitates efficient ether and ester synthesis under mild conditions. The electron-deficient aromatic ring enhances reactivity toward soft nucleophiles, enabling selective functionalization in complex molecular architectures.
Phenyl p-toluenesulfonate serves as a reliable aryl sulfate ester for nucleophilic aromatic substitution and transesterification reactions. Its bench-stable nature and predictable reactivity enable efficient O- and C-arylation workflows, particularly in the synthesis of biaryl ethers and heterocyclic scaffolds. The tosyl group provides excellent leaving-group ability under mild conditions while maintaining compatibility with diverse functional groups.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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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-H318-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: