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-(Trimethylsilyl)Cyclopropyl Phenyl Sulfide CAS NO 74379-74-1

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CAS No.:74379-74-1

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Content:99.90%

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1,1-Diphenyl-1-Propene-2-Thiol CAS NO 74630-83-4

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CAS No.:74630-83-4

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Α-Methyl-Α-Phenylbenzenemethanethiol CAS NO 74630-84-5

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CAS No.:74630-84-5

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4-tert-Butyl-2-Nitrobenzenethiol CAS NO 74752-38-8

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CAS No.:74752-38-8

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.Beta.-D-Glucopyranosiduronic Acid, Phenyl 1-Thio-, Ethyl Ester, Triacetate CAS NO 74774-12-2

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CAS No.:74774-12-2

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4-(3-Methoxypropyl)-4H-1,2,4-Triazole-3-Thiol CAS NO 75028-28-3

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CAS No.:75028-28-3

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Methoxybutyl 3-Mercaptopropionate CAS NO 75033-29-3

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CAS No.:75033-29-3

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2,5-Diamino-1,4-Benzenedithiol Dihydrochloride CAS NO 75464-52-7

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CAS No.:75464-52-7

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