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.

n-Succinimidyl-5-(2-Pyridyldithio)Valerate CAS NO 317331-86-5

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CAS No.:317331-86-5

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n-(2-Mercaptoethyl)-1,3-Thiazolidine CAS NO 317803-03-5

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CAS No.:317803-03-5

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5-Bromo-2-Fluoro-Benzenethiol CAS NO 321596-25-2

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CAS No.:321596-25-2

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4-Allyl-5-(3-Methylphenyl)-4H-1,2,4-Triazole-3-Thiol CAS NO 322412-27-1

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CAS No.:322412-27-1

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4,4'-(Ethyne-1,2-Diyl)Dibenzenethiol CAS NO 322639-14-5

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CAS No.:322639-14-5

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4-Methylphenyl 4,6-o-Benzylidene-2,3-Di-o-Benzoyl-1-Thio-Β-D-Glucopyranoside CAS NO 323195-40-0

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CAS No.:323195-40-0

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2,6-Piperidinedithione, 1-(4-Methyl-4-Pentenyl)- (9Ci) CAS NO 325956-84-1

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CAS No.:325956-84-1

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Ethanone, 1-[(1R,2S,3R,4S)-3-Mercaptobicyclo[2.2.1]Hept-2-Yl]-, Rel- (9Ci) CAS NO 326794-69-8

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CAS No.:326794-69-8

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