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.

(3-Nitrobenzyl)Mercaptan 97 CAS NO 77472-39-0

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CAS No.:77472-39-0

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Content:99.90%

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2-(Tetrahydro-Pyran-2-Yloxy)-Ethanethiol CAS NO 77597-08-1

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CAS No.:77597-08-1

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4-Bromo-2-(Trimethylsilyl)Thiophene CAS NO 77998-61-9

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CAS No.:77998-61-9

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Ethane, 1,1-Dimethoxy-2-[(2,2-Dimethoxyethyl)Thio]-] CAS NO 78102-16-6

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CAS No.:78102-16-6

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2-Propenoic Acid, 3-Amino-2-Cyano-3-Mercapto-, Methyl Ester CAS NO 78160-01-7

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CAS No.:78160-01-7

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3-(Methoxymethyl)-1H-1,2,4-Triazole-5-Thiol CAS NO 78201-12-4

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CAS No.:78201-12-4

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p-Mercaptoanilinium Chloride CAS NO 78749-58-3

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CAS No.:78749-58-3

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L-Proline,4-Mercapto-,Hydrochloride(1:1), CAS NO 78854-27-0

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CAS No.:78854-27-0

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