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.

2(1H)-Quinolinethione, 1-Ethyl-4,7-Dimethyl- CAS NO 53761-64-1

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CAS No.:53761-64-1

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Content:99.90%

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4-(4-Bromophenyl)-1,1,1-Trifluoro-4-Mercapto-3-Buten-2-One CAS NO 53833-48-0

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CAS No.:53833-48-0

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4-Methyl-1-Pentanethiol CAS NO 53897-50-0

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CAS No.:53897-50-0

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2-Mercaptopropionic Acid Methyl Ester CAS NO 53907-46-3

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CAS No.:53907-46-3

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2-Pyridinethiol,3,5-Dichloro-,1-Oxide(9Ci) CAS NO 53976-66-2

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CAS No.:53976-66-2

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Potassium Hydrogen 1,3,4-Thiadiazole-2,5-Dithiolate CAS NO 54092-09-0

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CAS No.:54092-09-0

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4-(2'-Naphthalenethio)-1,2-Phenylenediamine CAS NO 54092-93-2

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CAS No.:54092-93-2

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5-(2-Methylphenyl)-4H-1,2,4-Triazole-3-Thiol CAS NO 54294-18-7

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CAS No.:54294-18-7

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