Thiols/Thiophenols

Thiols/Thiophenols

Thiols and thiophenols are sulfur-containing organic reagents with strong nucleophilicity and characteristic odor. They participate in thiol-ene reactions, nucleophilic substitution, oxidation, metal binding, and polymer modification. Thiols are essential in bioconjugation, peptide chemistry, and redox biology due to their ability to form disulfide bonds. Thiophenols are used in pharmaceuticals, agrochemicals, and materials synthesis, particularly in forming thioethers and sulfur-functionalized aromatic compounds. Their metal-chelating ability supports catalyst formation and surface modification. Thiols also play roles in polymer crosslinking, vulcanization, and antioxidant chemistry. Their rich reactivity and biological relevance make thiols indispensable across chemical, biochemical, and materials science fields.

4-Chloro-2-Fluorobenzyl Mercaptan CAS NO 886498-25-5

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CAS No.:886498-25-5

Grade:Pharmacy Grade

Content:99.90%

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4-Bromo-2-Fluorobenzyl Mercaptan CAS NO 886498-29-9

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CAS No.:886498-29-9

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2,4,5-Trifluorobenzylmercaptan CAS NO 886498-39-1

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CAS No.:886498-39-1

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2-Benzyloxy-5-Acetaminobenzenethiol CAS NO 887352-92-3

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CAS No.:887352-92-3

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2-Benzyloxy-5-Nitrobenzenethiol CAS NO 887353-11-9

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CAS No.:887353-11-9

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2,2-Dimethyl-3-(4-Mercaptophenyl)Propionic Acid CAS NO 887354-80-5

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CAS No.:887354-80-5

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2-[(5-Fluoresceinyl)Aminocarbonyl]Ethyl Mercaptan CAS NO 887355-27-3

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CAS No.:887355-27-3

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Hexatriacontyl Methanethiosulfonate CAS NO 887406-39-5

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CAS No.:887406-39-5

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