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.

3-(Trifluoromethoxy)Thiophenol CAS NO 220239-66-7

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CAS No.:220239-66-7

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Content:99.90%

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2-Amino-5-Bromothiophenol CAS NO 220301-84-8

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CAS No.:220301-84-8

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20-(11-Mercaptoundecanoyl)-3,6,9,12,18-Hexaoxaeicosanoicacid CAS NO 221222-49-7

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CAS No.:221222-49-7

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2-Pyrrolidinemethanethiol,1-Ethyl-,(2S)-(9Ci) CAS NO 222856-54-4

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CAS No.:222856-54-4

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Cyclohexanethiol,5-Methyl-2-(1-Methylethyl)-,(1R,2R,5S)-Rel-(9Ci) CAS NO 223653-15-4

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CAS No.:223653-15-4

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Cyclohexanethiol,2-(1-Methylethyl)-,(1R,2R)-Rel-(9Ci) CAS NO 223653-39-2

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CAS No.:223653-39-2

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2-Pyrrolidinethione, 1-[2-(Hydroxymethyl)Phenyl]- CAS NO 224300-28-1

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CAS No.:224300-28-1

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3-Thiophenecarboxamide, 4-(Acetylamino)- CAS NO 224449-47-2

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CAS No.:224449-47-2

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