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-Mercapto-3-Methyl-1-Butyl-1-Formate CAS NO 50746-10-6

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CAS No.:50746-10-6

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Content:99.90%

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(Tetrahydrofuran-3-Yl)Methanethiol CAS NO 51171-23-4

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CAS No.:51171-23-4

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(4-Bromophenyl)Methyl Butyl-3-Pyridinylcarbonimidodithioate CAS NO 51308-80-6

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CAS No.:51308-80-6

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Butanoic Acid, 2-Mercapto-3-Oxo- (9Ci) CAS NO 51338-34-2

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CAS No.:51338-34-2

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p-Aminobenzyl-1-Thio-2-Acetamido-2-Deoxy -B-D-Gluco CAS NO 51450-14-7

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CAS No.:51450-14-7

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1-(3-Methoxyphenyl)-1H-Imidazole-2-Thiol CAS NO 51581-49-8

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CAS No.:51581-49-8

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4-(Mercaptomethyl)Benzonitrile CAS NO 51776-12-6

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CAS No.:51776-12-6

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1,4-Dimercapto Phthalazine CAS NO 51793-94-3

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CAS No.:51793-94-3

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