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.

(S)-2-Hydroxybutyl p-Tosylate CAS NO 143731-32-2

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CAS No.:143731-32-2

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Content:99.90%

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Toluene-4-Sulfonic Acid 2-(2-Benzyloxycarbonylamino-Ethoxy)-Ethyl Ester CAS NO 144208-62-8

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CAS No.:144208-62-8

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(1R,2R)-(-)-n-p-Tosyl-1,2-Diphenylethylenediamine CAS NO 144222-34-4

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CAS No.:144222-34-4

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5-Ethyl-2-Pyridineethanol Tosylate CAS NO 144809-27-8

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CAS No.:144809-27-8

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Propargyl-Peg2-Tos CAS NO 145916-41-2

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CAS No.:145916-41-2

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2-(Tosyloxy)Cycloheptanone CAS NO 146040-84-8

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CAS No.:146040-84-8

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Arecaidine Propargyl Ester Tosylate CAS NO 147202-94-6

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CAS No.:147202-94-6

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Tosylthreonylglycine Methyl Ester CAS NO 151656-28-9

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CAS No.:151656-28-9

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