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.

1-p-Tolyl-1H-Tetrazole-5-Thiol CAS NO 13980-77-3

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CAS No.:13980-77-3

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Content:99.90%

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.Alpha.-D-Glucopyranoside, Phenyl 1-Thio- CAS NO 13992-15-9

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CAS No.:13992-15-9

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.Alpha.-D-Glucopyranoside, Phenyl 1-Thio-, Tetraacetate CAS NO 13992-16-0

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CAS No.:13992-16-0

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2-Bromo-5-Methoxybenzenethiol CAS NO 13993-51-6

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CAS No.:13993-51-6

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1-[2-(2-Furyl)-4-Mercapto-6-Methylpyrimidin-5-Yl]Ethanone CAS NO 13995-71-6

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CAS No.:13995-71-6

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trans-4,5-Dihydroxy-1,2-Dithiane CAS NO 14193-38-5

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CAS No.:14193-38-5

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Acetone Diethyl Dithioacetal CAS NO 14252-45-0

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CAS No.:14252-45-0

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3-Mercapto-2-(Methylamino)Propanoic Acid Hydrochloride CAS NO 14344-46-8

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CAS No.:14344-46-8

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