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.

Ethanethione, 2-(2-Chlorophenyl)-1-(4-Morpholinyl)- CAS NO 159298-85-8

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CAS No.:159298-85-8

Grade:Pharmacy Grade

Content:99.90%

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Α-D-Mannopyranoside, Phenyl 2,3-Bis-o-(Phenylmethyl)-4,6-o-[(R)-Phenylmethylene]-1-Thio- CAS NO 159407-17-7

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CAS No.:159407-17-7

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Phenyl 4,6-o-Benzylidene-1-Thio-A-D-Mannopyranoside CAS NO 159407-19-9

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CAS No.:159407-19-9

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2-Thiophenethiol,5-Amino-(9Ci) CAS NO 159504-43-5

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CAS No.:159504-43-5

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Heptakis-(6-Mercapto-6-Deoxy)-Beta-Cyclodextrin CAS NO 160661-60-9

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CAS No.:160661-60-9

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2-Butanethiol,1-(Dimethylamino)-(9Ci) CAS NO 160978-96-1

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CAS No.:160978-96-1

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2-Dimethylaminoethanethiol Hydrochloride CAS NO 161909-82-6

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CAS No.:161909-82-6

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Methylmercapto-2,3,4,6-Tetra-o-Benzyl-D-Mannopyranoside CAS NO 162061-34-9

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CAS No.:162061-34-9

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