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.

1,1'-Dithiobis(3,5,7-Trimethyl-2,4,6,8-Tetrathiaadamantane) CAS NO 57274-54-1

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CAS No.:57274-54-1

Grade:Pharmacy Grade

Content:99.90%

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5-(4-Methoxyphenyl)-4-Methyl-4H-1,2,4-Triazole-3-Thiol CAS NO 57295-83-7

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CAS No.:57295-83-7

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p-(Trimethylsilyl)Phenylmethanethiol CAS NO 57337-85-6

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CAS No.:57337-85-6

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n-(1,3,2,4-Dithiadiazol-3-Siv-5-Ylidene)-p-Methylbenzamide CAS NO 57726-52-0

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CAS No.:57726-52-0

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2,3,5-Trichlorothiophenol CAS NO 57730-97-9

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CAS No.:57730-97-9

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2,4,6-Tribromothiophenol CAS NO 57730-98-0

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CAS No.:57730-98-0

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2-Mercaptoethyl Octanoate CAS NO 57813-59-9

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CAS No.:57813-59-9

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(S)-(-)-Thiolactic Acid CAS NO 57965-30-7

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CAS No.:57965-30-7

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