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.

Benzenemethanethiol, 3,5-Dimethoxy- CAS NO 346419-41-8

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CAS No.:346419-41-8

Grade:Pharmacy Grade

Content:99.90%

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4-Amino-5-(4-tert-Butyl-Phenyl)-4H-[1,2,4]Triazole-3-Thiol CAS NO 349116-17-2

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CAS No.:349116-17-2

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4-Bromo-Alpha-Toluene Thiolacetate 97 CAS NO 351003-15-1

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CAS No.:351003-15-1

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3-Chloro-2-Nitrobenzenethiol CAS NO 351216-87-0

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CAS No.:351216-87-0

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5-Aminopentyl Methanthiosulfonate Hydrobromide CAS NO 351422-76-9

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CAS No.:351422-76-9

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Content:99.90%

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Benzenediamidoethanethiol N,N'-Bis(2-Mercaptoethyl)Isophthalamide CAS NO 351994-94-0

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CAS No.:351994-94-0

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Content:99.90%

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Α-D-Arabinofuranoside, 4-Methylphenyl 1-Thio-, 2,3,5-Tribenzoate CAS NO 352438-38-1

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CAS No.:352438-38-1

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Content:99.90%

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3-Thiophenecarboxylic Acid, 2-[(3-Chloro-1-Oxopropyl)Amino]-4-Phenyl-, Ethyl Ester CAS NO 355003-70-2

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CAS No.:355003-70-2

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Content:99.90%

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