Thiol Esters

Thiol Esters

Thiol esters are sulfur-containing acyl-transfer reagents widely used in peptide synthesis, native chemical ligation, and biological chemistry. Their high reactivity toward nucleophiles enables efficient formation of amides, thioesters, and activated acyl intermediates. Thiol esters participate in enzymatic processes, including fatty-acid activation and CoA-mediated metabolism. In organic synthesis, they support acylation, reduction, radical reactions, and decarboxylative coupling. Their enhanced stability relative to acyl halides allows controlled reactivity in multistep processes. Thiol esters play a critical role in biomimetic transformations and advanced peptide-engineering strategies.

4-((((2-Carboxyethyl)Thio)Carbonothioyl)Thio)-4-Cyanopentanoic Acid CAS NO 2055041-03-5

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CAS No.:2055041-03-5

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Content:99.90%

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Diethyldithiocarbamic Acid Benzyl Ester CAS NO 3052-61-7

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CAS No.:3052-61-7

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Phenylthiocarbamic Acid Ethyl Ester CAS NO 3111-89-5

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CAS No.:3111-89-5

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Acetyl Sulfide CAS NO 3232-39-1

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CAS No.:3232-39-1

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3-Methoxy-Phenylthioaceticacid CAS NO 3996-32-5

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CAS No.:3996-32-5

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Isooctyl 3-Mercaptopropionate CAS NO 30374-01-7

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CAS No.:30374-01-7

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Phenyl Thioacetate CAS NO 30623-40-6

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CAS No.:30623-40-6

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S-(4-Chlorophenyl) 3-(1,3-Benzodioxol-5-Yl)-2-Propenethioate CAS NO 298215-57-3

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CAS No.:298215-57-3

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