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.

Cyclohexyl Mercaptoacetate CAS NO 16849-98-2

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CAS No.:16849-98-2

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3,4-Dichlorothiophenol CAS NO 17231-17-3

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CAS No.:17231-17-3

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3,5-Dichlorothiophenol CAS NO 17231-94-6

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CAS No.:17231-94-6

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3-Chloro-2-Methylthiophene CAS NO 17249-83-1

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CAS No.:17249-83-1

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2,2'-Dithiobis(N,n-Dimethylethylamine) Dihydrochloride CAS NO 17339-60-5

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CAS No.:17339-60-5

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2-Ethoxyethanethiol CAS NO 17362-04-8

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CAS No.:17362-04-8

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1,3,5,7,10-Pentamethyl-2,4,6,8,9-Pentathiaadamantane CAS NO 17443-93-5

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CAS No.:17443-93-5

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1,5,10,10-Tetramethyl-2,4,6,8,9-Pentathiaadamantane CAS NO 17443-96-8

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CAS No.:17443-96-8

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