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.

n-(2-Mercaptoethyl) Demecolcine CAS NO 1217746-74-1

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CAS No.:1217746-74-1

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1-Bromo-3,5-Dimercaptobenzene CAS NO 1219501-75-3

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CAS No.:1219501-75-3

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1-Boc-3-(Mercaptomethyl)-Azetidine CAS NO 1236007-18-3

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CAS No.:1236007-18-3

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(R)-(1-Mercaptomethyl-2-Phenyl-Ethyl)-Carbamic Acid tert-Butyl Ester CAS NO 1217604-63-1

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CAS No.:1217604-63-1

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(R)-2-Mercaptobutanoic Acid CAS NO 1242881-37-3

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CAS No.:1242881-37-3

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2-Fluoro-3-Methylbenzenethiol, 2-Fluoro-m-Tolyl Mercaptan CAS NO 1243283-09-1

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CAS No.:1243283-09-1

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5-Fluoro-2-Methylthiophenol CAS NO 1243442-20-7

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CAS No.:1243442-20-7

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6-Bromo-2-Mercaptobenzo[D]Thiazole-5-Carbonitrile CAS NO 1242336-64-6

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CAS No.:1242336-64-6

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