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-(4-Bromophenyl)-1-(4-Methylphenyl)-1H-Imidazole-2-Thiol CAS NO 1105189-65-8

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CAS No.:1105189-65-8

Grade:Pharmacy Grade

Content:99.90%

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2-[5-(Hydroxymethyl)-2-Mercapto-1H-Imidazol-1-Yl]-n-(4-Methylbenzyl)Acetamide CAS NO 1105190-15-5

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CAS No.:1105190-15-5

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1-(1,3-Benzodioxol-5-Ylmethyl)-1H-Imidazole-2-Thiol CAS NO 1105195-60-5

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CAS No.:1105195-60-5

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3-Chloro-2-Fluorobenzenethiol CAS NO 1121585-29-2

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CAS No.:1121585-29-2

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4-Pyridinemethanethiol, Α-Phenyl- CAS NO 1154888-05-7

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CAS No.:1154888-05-7

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[7-(Trimethylammonium)Hepyl] Methanethiosulfonate Bromide CAS NO 1159174-26-1

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CAS No.:1159174-26-1

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2-(3,5-Dichlorophenyl)Ethanethiol CAS NO 1174005-49-2

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CAS No.:1174005-49-2

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Content:99.90%

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(2S,4S)-1-n-Cbz-4-Mercaptopyrrolidine-2-Carboxylic Acid Benzyl Ester CAS NO 1176446-09-5

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CAS No.:1176446-09-5

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