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.

Benzenesulfonamide, 4-Mercapto- (9Ci) CAS NO 64058-62-4

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CAS No.:64058-62-4

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Content:99.90%

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L-Cysteine,S-[4,6-Bis(Dimethylamino)-1,3,5-Triazin-2-Yl]- CAS NO 64124-19-2

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CAS No.:64124-19-2

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Chembrdg-Bb 5685442 CAS NO 64375-68-4

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CAS No.:64375-68-4

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4′-Mercapto-[1,1′-Biphenyl]-4-Carbonitrile CAS NO 64409-12-7

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CAS No.:64409-12-7

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1,7-Dicarba-Closo-Dodecaborane-9-Yl-Thiol, 9-Mercapto-1,7-Dicarbadodecaborane (12) CAS NO 64493-44-3

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CAS No.:64493-44-3

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Potassium 3-Mercaptopropionate CAS NO 65086-45-5

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CAS No.:65086-45-5

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3,4,4A,5,6,10B-Hexahydro-2,4-Diphenyl-2H-Naphtho(1,2-B)Thiopyran CAS NO 65193-64-8

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CAS No.:65193-64-8

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.Alpha.-D-Glucopyranoside, Phenyl 1-Thio-, Tetrabenzoate CAS NO 65236-86-4

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CAS No.:65236-86-4

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