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-[[(4-Methoxyphenyl)Thioxomethyl]Thio]Butyric Acid Methyl Ester CAS NO 36122-41-5

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CAS No.:36122-41-5

Grade:Pharmacy Grade

Content:99.90%

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2-(Benzoylamino)-2-Mercaptopropionic Acid Methyl Ester CAS NO 36648-51-8

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CAS No.:36648-51-8

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o-(tert-Butyl) S-Phenyl Thiocarbonate CAS NO 36760-43-7

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CAS No.:36760-43-7

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(-)-Thioacetic Acid S-(3-Acetoxy-5-Undecenyl) Ester CAS NO 36948-67-1

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CAS No.:36948-67-1

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Ethanethioic Acid, S,S-(2,3-Dihydroxy-1,4-Butanediyl) Ester CAS NO 37180-64-6

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CAS No.:37180-64-6

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Enzacryl(R) Polythiolactone* CAS NO 37265-18-2

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CAS No.:37265-18-2

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10(9H)-Acridinecarbothioic Acid, 9,9-Dimethyl-, S-(2-(4-Methyl-1-Piper Azinyl)Ethyl) Ester CAS NO 38044-66-5

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CAS No.:38044-66-5

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Heptyl Mercaptoacetate CAS NO 39583-10-3

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CAS No.:39583-10-3

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Content:99.90%

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