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.

2-Chloromethyl-1,3-Dithiolane CAS NO 86147-22-0

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CAS No.:86147-22-0

Grade:Pharmacy Grade

Content:99.90%

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Purine-6-Sulfenic Acid CAS NO 86335-59-3

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CAS No.:86335-59-3

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Methylsulfenyliodide CAS NO 86381-89-7

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CAS No.:86381-89-7

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1-(2-Diethylaminoethyl)-5-Mercaptotetrazole CAS NO 86475-43-6

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CAS No.:86475-43-6

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1-Thio-4-Chromanone-2-Acetic Acid CAS NO 86628-18-4

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CAS No.:86628-18-4

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3-Ethoxy Thiophenol CAS NO 86704-82-7

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CAS No.:86704-82-7

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1,5-Dithiacyclooctan-3-Ol CAS NO 86944-00-5

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CAS No.:86944-00-5

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Content:99.90%

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Ethanone, 2,2,2-Trifluoro-1-(4-Mercaptophenyl)- (9Ci) CAS NO 86988-51-4

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CAS No.:86988-51-4

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