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.

(L-Leucinethiol)2 2 Hcl CAS NO 112157-33-2

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CAS No.:112157-33-2

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Content:99.90%

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Imidazo[1,2-A]Pyrazine-5-Thiol CAS NO 112266-79-2

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CAS No.:112266-79-2

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3-Mercapto-n-(2-Mercaptoethyl)Propanamide CAS NO 112806-12-9

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CAS No.:112806-12-9

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2-Propanone, 1-[(1-Methylethyl)Thio]- (9Ci) CAS NO 112988-41-7

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CAS No.:112988-41-7

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3-Allyl-2-Mercapto-3,5,6,7-Tetrahydro-4H-Cyclopenta[4,5]Thieno[2,3-D]Pyrimidin-4-One CAS NO 113520-01-7

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CAS No.:113520-01-7

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D-Cysteine, S-2-Pyridinyl- (9Ci) CAS NO 113828-61-8

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CAS No.:113828-61-8

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6H-Imidazo[4,5-E]Benzothiazole-7-Thiol,2-Methyl-(6Ci) CAS NO 114163-54-1

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CAS No.:114163-54-1

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4(1H)-Pyridinethione,1-(1-Methylethyl)-(9Ci) CAS NO 114588-77-1

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CAS No.:114588-77-1

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