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-Ethyl-5-Thiolato-3-Methyl-1,2,3-Thiadiazol-3-Ium CAS NO 56701-32-7

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CAS No.:56701-32-7

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Content:99.90%

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5-Thiolato-4-Methyl-3-Phenyl-1,2,3-Thiadiazol-3-Ium CAS NO 56793-03-4

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CAS No.:56793-03-4

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5-Thiolato-3,4-Diphenyl-1,2,3-Thiadiazol-3-Ium CAS NO 56909-20-7

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CAS No.:56909-20-7

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2-(5-Mercapto-1,3,4-Thiadiazol-2-Ylthio)-Ethanol CAS NO 57037-59-9

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CAS No.:57037-59-9

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Hydroxydec-2-Enoic Acid Ethyl Ester, (E)-10-(Sh) CAS NO 57221-93-9

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CAS No.:57221-93-9

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Methanetrithioletriacetate CAS NO 57274-27-8

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CAS No.:57274-27-8

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3,5,7-Trimethyl-2,4,6,8,9-Pentathiaadamantane-1-Thiol CAS NO 57274-31-4

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CAS No.:57274-31-4

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3,5,7-Trimethyl-2,4,6,8-Tetrathiaadamantane-1-Thiol CAS NO 57274-35-8

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CAS No.:57274-35-8

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