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-Mercapto-1-Adamantanecarboxylic Acid CAS NO 247225-76-9

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CAS No.:247225-76-9

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Content:99.90%

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3,4-(Ethylenedioxy)Thiophenol CAS NO 247228-28-0

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CAS No.:247228-28-0

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Hs-Peg5-Oh CAS NO 248582-03-8

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CAS No.:248582-03-8

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2-Pyrrolidinethione, 1-(2-Mercaptoethyl)- CAS NO 251318-68-0

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CAS No.:251318-68-0

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2-(3-Sulfanylpropyl)Pentanedioic Acid CAS NO 254737-29-6

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CAS No.:254737-29-6

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Aabd-Sh CAS NO 254973-02-9

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CAS No.:254973-02-9

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Cyclopentaneacetic Acid, -Alpha--Amino-1-Mercapto-, (-Alpha-R)- (9Ci) CAS NO 255052-59-6

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CAS No.:255052-59-6

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L-Proline, 2-Mercapto- (9Ci) CAS NO 255052-61-0

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CAS No.:255052-61-0

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