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.

(S)-3-Mercapto-Pyrrolidine-1-Carboxylic Acid tert-Butyl Ester CAS NO 156371-85-6

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CAS No.:156371-85-6

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Content:99.90%

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2-Hexanone, 5-Mercapto- (9Ci) CAS NO 156386-62-8

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CAS No.:156386-62-8

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(R)-4-Mercapto-2-Pyrrolidone CAS NO 157429-42-0

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CAS No.:157429-42-0

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(2-Bromoethyl)(Trityl)Sulfane CAS NO 157522-54-8

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CAS No.:157522-54-8

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Pyrrolo[1,2-A]Pyrazin-1(2H)-One, Hexahydro-7-Mercapto-4-Methyl-, [4R-(4-Alpha-,7-Alpha-,8A-Ba-)]- (9Ci) CAS NO 158393-29-4

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CAS No.:158393-29-4

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2-(2-Pyridinylamino)-Benzenethiol CAS NO 158438-81-4

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CAS No.:158438-81-4

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n-Acetyl-S-(4-Hydroxy-2-Buten-1-Yl)- CAS NO 159092-65-6

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CAS No.:159092-65-6

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(1-Methyl-1H-Benzoimidazol-2-Ylsulfanyl)-Acetic Acid CAS NO 159222-24-9

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CAS No.:159222-24-9

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