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.

4-(4-Chloro-Phenyl)-1,3-Dihydro-Imidazole-2-Thione CAS NO 93103-18-5

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CAS No.:93103-18-5

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Content:99.90%

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1,3-Thiazetidine,3-(1-Methylethyl)-2-(Nitromethylene)-(9Ci) CAS NO 93243-23-3

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CAS No.:93243-23-3

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Carbamic Acid, (3-Mercaptopropyl)-, 1,1-Dimethylethyl Ester (9Ci) CAS NO 93472-93-6

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CAS No.:93472-93-6

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3-Methyl-1-(Phenylsulfanyl)Butan-1-One CAS NO 93500-17-5

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CAS No.:93500-17-5

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3-Phenyl-3-Methyl-2-Mercaptopropenoic Acid CAS NO 93628-49-0

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CAS No.:93628-49-0

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4,5-Dimethyl-2-(2-(Methylthio)Ethyl)-1,3-Dithiolane CAS NO 93788-31-9

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CAS No.:93788-31-9

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7-Methyl-Benzooxazole-2-Thiol CAS NO 93794-43-5

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CAS No.:93794-43-5

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4-Methyl-1,3-Benzoxazole-2-Thiol CAS NO 93794-44-6

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CAS No.:93794-44-6

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