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.

2-Ethylhexyl 3-Mercaptopropionate CAS NO 50448-95-8

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CAS No.:50448-95-8

Grade:Pharmacy Grade

Content:99.00%

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Benzenethiosulfonic Acid S-Phenyl Ester CAS NO 1212-08-4

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CAS No.:1212-08-4

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Content:99.0%

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Thioacetic Acid S-[p-[Bis(2-Chloroethyl)Amino]Phenyl] Ester CAS NO 1507-07-9

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CAS No.:1507-07-9

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Content:99.90%

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Dimethyl Mercaptosuccinate CAS NO 1795-56-8

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CAS No.:1795-56-8

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Content:99.90%

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Dibenzoic Thioanhydride CAS NO 1850-15-3

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CAS No.:1850-15-3

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Content:99.90%

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Pertrithiobis(Thioformic Acid o-Ethyl) Ester CAS NO 1851-77-0

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CAS No.:1851-77-0

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Content:99.90%

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p-Nitrophenyldithiocarbamic Acid Ethyl Ester CAS NO 13037-41-7

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CAS No.:13037-41-7

Grade:Pharmacy Grade

Content:99.90%

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Methyl 2-Pyridinyldithiocarbamate CAS NO 13037-46-2

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CAS No.:13037-46-2

Grade:Pharmacy Grade

Content:99.90%

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