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.

R- 4-(1-Methylethyl)-3-(1-Oxopropyl)-2-Thiazolidinethione CAS NO 487029-68-5

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CAS No.:487029-68-5

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Content:99.90%

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5-(4-Bromo-Phenyl)-4-Methyl-4 H-[1,2,4]Triazole-3-Thiol CAS NO 494194-50-2

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CAS No.:494194-50-2

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20-(11-Mercaptoundecanyloxy)-3,6,9,12,15,18-Hexaoxaeicosane-1-Amine,Hydrochloride CAS NO 496839-01-1

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CAS No.:496839-01-1

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Benzenethiol, 4-Amino-2-Methoxy- (9Ci) CAS NO 497855-25-1

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CAS No.:497855-25-1

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Benzenethiol, 2-?Methyl-?4-?Nitro- CAS NO 497855-56-8

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CAS No.:497855-56-8

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Propanoic Acid, 3-[[[(Phenylmethyl)Thio]Thioxomethyl]Thio]- CAS NO 497931-76-7

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CAS No.:497931-76-7

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1,2-Ethanediyl Bismethanethiosulfonate CAS NO 55-95-8

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CAS No.:55-95-8

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S-[2-(Diethylamino)Ethyl] Diphenyldithiocarbamate Monohydrochloride CAS NO 58-13-9

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CAS No.:58-13-9

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Content:99.90%

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