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-Ethoxy-2-Mercaptobenzimidazole CAS NO 55489-15-1

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CAS No.:55489-15-1

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Content:99.90%

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2-(Dibenzylamino)Ethanethiol CAS NO 55415-31-1

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CAS No.:55415-31-1

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Benzoic Acid, 4-Amino-3-Mercapto-, Ethyl Ester CAS NO 55439-71-9

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CAS No.:55439-71-9

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1-Mercaptohexadecan-2-Ol CAS NO 55525-35-4

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CAS No.:55525-35-4

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3-(4-Acetylphenyl)-3-Hydroxypropenedithioic Acid CAS NO 55538-72-2

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CAS No.:55538-72-2

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1,1,1-Trifluoro-4-Mercapto-4-Phenyl-3-Buten-2-One CAS NO 55674-00-5

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CAS No.:55674-00-5

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1,1,1-Trifluoro-4-Mercapto-4-(4-Methylphenyl)-3-Buten-2-One CAS NO 55674-02-7

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CAS No.:55674-02-7

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3-(1,3-Dithian-2-Ylidene)-Pentane-2,4-Dione CAS NO 55727-23-6

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CAS No.:55727-23-6

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