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.

1-Chloro-3-Mercapto-2-Propanol CAS NO 6478-04-2

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CAS No.:6478-04-2

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Propanamide, n-(2-Amino-2-Oxoethyl)-2-Mercapto- CAS NO 6513-25-3

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CAS No.:6513-25-3

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L-Rhamnose Diethylmercaptal CAS NO 6748-70-5

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CAS No.:6748-70-5

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2H-Thiopyran-3,5(4H,6H)-Dione CAS NO 6881-49-8

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CAS No.:6881-49-8

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2-Mercapto-5-Thiazolidone CAS NO 6913-23-1

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CAS No.:6913-23-1

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Galactose, Diethyl Mercaptal, Pentaacetate, D- CAS NO 6935-10-0

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CAS No.:6935-10-0

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Biphenyl-4,4'-Dithiol CAS NO 6954-27-4

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CAS No.:6954-27-4

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2H-Benzo[4,5]Thiazolo[2,3-C][1,2,4]Triazole-3-Thione CAS NO 6957-85-3

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CAS No.:6957-85-3

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