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.

S-Butyl 4-Bromothiophenol CAS NO 121392-35-6

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CAS No.:121392-35-6

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Content:99.90%

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N,n-Dimethyl-2-Mercaptonicotinamide CAS NO 121650-19-9

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CAS No.:121650-19-9

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5-[2-(3,4-Dimethoxyphenyl)Ethyl]-4-Phenyl-4H-1,2,4-Triazole-3-Thiol CAS NO 121670-52-8

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CAS No.:121670-52-8

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S-n-Hexyl-D-Cysteine CAS NO 121961-52-2

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CAS No.:121961-52-2

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Pyridine-2-Thiol Hydrochloride CAS NO 123574-75-4

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CAS No.:123574-75-4

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Benzothiazole, 2-(Oxiranylthio)- (9Ci) CAS NO 123708-28-1

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CAS No.:123708-28-1

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1,1-Binaphthalene-2,2-Dithiol, (1S)- CAS NO 124414-36-4

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CAS No.:124414-36-4

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1,1-Binaphthalene-2,2-Dithiol, (1R)- CAS NO 124414-37-5

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CAS No.:124414-37-5

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