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.

Pyrimidine, 2-(Ethylthio)- (7Ci,8Ci,9Ci) CAS NO 10132-25-9

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CAS No.:10132-25-9

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Content:99.90%

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2-(1,2,2-Trimethylpropoxy)Ethanethiol CAS NO 10160-73-3

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CAS No.:10160-73-3

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Methanamine, 1-(2-Benzothiazolylthio)-N,n-Dimethyl- (9Ci) CAS NO 10220-35-6

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CAS No.:10220-35-6

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4,5-Bis(Mercaptomethyl)-o-Xylene CAS NO 10230-61-2

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CAS No.:10230-61-2

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3-Methyl-4-Pyridinethiol CAS NO 10351-13-0

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CAS No.:10351-13-0

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5-Thio-D-Glucopyranose 1,2,3,4,6-Pentaacetate CAS NO 10470-80-1

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CAS No.:10470-80-1

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5-([2-[(5-Mercapto-1,3,4-Thiadiazol-2-Yl)Thio]Ethyl]Thio)-1,3,4-Thiadiazole-2-Thiol CAS NO 10486-54-1

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CAS No.:10486-54-1

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3-Benzylrhodanine CAS NO 10574-69-3

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CAS No.:10574-69-3

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