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.

3-(p-Toluenesulfonate)-n-Methyl-n-Boc-Propylamine CAS NO 200563-87-7

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CAS No.:200563-87-7

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Content:99.90%

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m-Peg10-Tos CAS NO 211859-75-5

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CAS No.:211859-75-5

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Content:99.90%

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(1S,2S)-(-)-N,n-Di-p-Tosyl-1,2-Cyclohexanediamine CAS NO 212555-28-7

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CAS No.:212555-28-7

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Hexatosylate Dipentaerylthritol CAS NO 214144-11-3

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CAS No.:214144-11-3

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3,5,10,12,17,19,24,26-Octakis-Tosyloxy-1,8,15,22-Tetramethyl[4!Resorcinolarene CAS NO 214358-32-4

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CAS No.:214358-32-4

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Trt-Peg4-Otos CAS NO 223611-40-3

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CAS No.:223611-40-3

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Content:99.90%

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L-Glycero-L-Galacto-Heptitol, 2,6-Anhydro-3,4-o-(1-Methylethylidene)-7-Thio-, 1-(4-Methylbenzenesulfonate) CAS NO 228115-87-5

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CAS No.:228115-87-5

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Benzenepropanol, 5-Bromo-G-Phenyl-2-(Phenylmethoxy)-, 4-Methylbenzenesulfonate (9Ci) CAS NO 250214-37-0

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CAS No.:250214-37-0

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Content:99.90%

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