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-(3-Aminopropyl)Thiosulfuric Acid Ester CAS NO 13286-24-3

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CAS No.:13286-24-3

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Ammonium 2-Mercaptopropionate CAS NO 13419-67-5

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CAS No.:13419-67-5

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Alanine, n-Acetyl-3-((3,4-Dichlorophenyl)Thio)- CAS NO 13443-69-1

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CAS No.:13443-69-1

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3-Chlorophenylthioethanol CAS NO 13457-99-3

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CAS No.:13457-99-3

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1H-Pyrrolo[1,2-C]Imidazole-1,5(6H)-Dione,3-Mercapto-7-Methyl-(8Ci) CAS NO 13594-06-4

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CAS No.:13594-06-4

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6-Benzothiazolol(7Ci,8Ci,9Ci) CAS NO 13599-84-3

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CAS No.:13599-84-3

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4-Methyl-2,3,5,6-Tetrafluorothiophenol CAS NO 13634-89-4

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CAS No.:13634-89-4

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1,4-Di(2'-Thienyl)-1,4-Butadione CAS NO 13669-05-1

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CAS No.:13669-05-1

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