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.

5-Mercapto-4-Phenyl-3H-1,2-Dithiole-3-Thione CAS NO 16101-90-9

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CAS No.:16101-90-9

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Content:99.90%

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Pyridine-3-Thiol CAS NO 16133-26-9

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CAS No.:16133-26-9

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5H-Cyclopenta-p-Dithiin,Hexahydro-,cis-(8Ci) CAS NO 16214-58-7

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CAS No.:16214-58-7

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Bis-(2-Methanethiosulfonatoethyl)Methylamine CAS NO 16216-82-3

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CAS No.:16216-82-3

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1-Tetracosanthiol CAS NO 16331-24-1

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CAS No.:16331-24-1

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3-Amino-5-Mercapto-1,2,4-Triazole CAS NO 16691-43-3

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CAS No.:16691-43-3

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1,2:3,4-Di-o-Isopropylidene-6-Thio-A-D-Galactopyranose CAS NO 16714-07-1

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CAS No.:16714-07-1

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2-(Phenylthio)Thiophene CAS NO 16718-12-0

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CAS No.:16718-12-0

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