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.

3,4-Methylenedioxybenzyl Mercaptan CAS NO 34817-07-7

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CAS No.:34817-07-7

Grade:Pharmacy Grade

Content:99.90%

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n-[(Chlorodifluoromethyl)Dithio]-Α,Α-Dichloromethanimine CAS NO 35075-14-0

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CAS No.:35075-14-0

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(2R,5S)-2-(1-Mercapto-1-Methylethyl)-5-Methylcyclohexanone CAS NO 35117-86-3

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CAS No.:35117-86-3

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Content:99.90%

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Bis(p-(Mewthoxycarbonyl)Phenyl)Disulfide CAS NO 35190-68-2

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CAS No.:35190-68-2

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Content:99.90%

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2-Pyrazinylethanethiol CAS NO 35250-53-4

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CAS No.:35250-53-4

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3'-Mercaptoacetophenone CAS NO 35337-69-0

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CAS No.:35337-69-0

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Content:99.90%

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5-Methyl-[1,2,4]Triazolo[4,3-A]Quinoline-1-Thiol CAS NO 35359-27-4

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CAS No.:35359-27-4

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Content:99.90%

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2-(4-Bromophenoxy)Ethanethioamide(Wx191949) CAS NO 35368-49-1

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CAS No.:35368-49-1

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Content:99.90%

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