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.

5-(2,4-Dichlorophenyl)-4-Ethyl-4H-1,2,4-Triazole-3-Thiol CAS NO 29527-30-8

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CAS No.:29527-30-8

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Content:99.90%

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1-(2-Mercaptoethyl)-5-Phenyluracil CAS NO 29558-48-3

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CAS No.:29558-48-3

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Methyl (Methyl 1-Thio-2,3,4-Tri-o-Acetyl-Beta-D-Glucopyranosid)-Uronate CAS NO 29587-10-8

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CAS No.:29587-10-8

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5-Pyrimidinethiol (8Ci,9Ci) CAS NO 29878-64-6

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CAS No.:29878-64-6

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2-Mercaptoethyl Myristate CAS NO 29946-28-9

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CAS No.:29946-28-9

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1,1'-[Isopropylidenebis(p-Phenyleneoxy)]Bis[3-Mercaptopropan-2-Ol] CAS NO 29953-09-1

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CAS No.:29953-09-1

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1H-Benzimidazole-2-Propanethiol(9Ci) CAS NO 29982-03-4

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CAS No.:29982-03-4

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2-[2-[2-(2-Mercaptoethoxy)Ethoxy]Ethoxy]Acetic Acid CAS NO 200291-35-6

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CAS No.:200291-35-6

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