Tosylates

Tosylates

Tosylates are highly versatile sulfonate ester reagents widely used as activated leaving groups, intermediates, and functional materials in organic synthesis. Derived from p-toluenesulfonyl chloride, tosylates convert alcohols into excellent electrophiles, enabling efficient nucleophilic substitution, elimination, reduction, and cross-coupling reactions. Their exceptional stability, predictable reactivity, and broad functional-group compatibility make tosylates key tools in multi-step synthesis, protecting-group strategies, and heterocycle construction. In pharmaceuticals and fine chemicals, tosylates serve as intermediates for amines, halides, thiols, ethers, and chiral building blocks. They also participate in polymer modification, phase-transfer processes, and catalytic transformations. Due to their tunable reactivity and reliable performance under mild conditions, tosylates remain indispensable in modern synthetic chemistry and industrial manufacturing.

1-(Trimethylsilyl)-1-Propyn-3-Yl Tosylate CAS NO 71321-16-9

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CAS No.:71321-16-9

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Content:99.90%

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(9H-Fluoren-9-Yl)Methyl 4-Methylbenzene-1-Sulfonate CAS NO 71532-40-6

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CAS No.:71532-40-6

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(2S,3S)-(-)-2,3-Butanediol Di-p-Tosylate CAS NO 74839-83-1

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CAS No.:74839-83-1

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Tetrahydro-2H-Pyran-2-Ylmethyl 4-Methylbenzenesulfonate CAS NO 75434-63-8

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CAS No.:75434-63-8

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Ethanol, 2-[2-(2-Hydroxyethoxy)Ethoxy]-, 1-(4-Methylbenzenesulfonate) CAS NO 77544-68-4

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CAS No.:77544-68-4

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2,3-Dihydrobenzofuran-5-Ethanol Tosylate CAS NO 79679-49-5

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CAS No.:79679-49-5

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Tos-Peg10-Ch2Ch2Cootbu CAS NO 778596-20-6

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CAS No.:778596-20-6

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Pentaethylene Glycol Mono Methyl Ether Tosylate CAS NO 80755-67-5

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CAS No.:80755-67-5

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