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-Mercaptoundec-11-Yl)Hexa(Ethylene Gl& CAS NO 130727-44-5

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CAS No.:130727-44-5

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B-D-Glucopyranoside, Phenyl 3,4,6-Tris-o-(Phenylmethyl)-1-Thio- CAS NO 130781-27-0

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CAS No.:130781-27-0

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3,5-Bis(Trifluoromethyl)Benzenethiol CAS NO 130783-02-7

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CAS No.:130783-02-7

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Benzenethiol, 2,3-Difluoro- (9Ci) CAS NO 130922-39-3

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CAS No.:130922-39-3

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n-(3-Mercapto-3-Methylbutyryl)-Beta-Alanine CAS NO 131068-51-4

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CAS No.:131068-51-4

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Benzenethiol, 2-Amino-5-(1-Methylethyl)- (9Ci) CAS NO 131105-91-4

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CAS No.:131105-91-4

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Benzenethiol, 2-Amino-4,5-Difluoro- (9Ci) CAS NO 131105-93-6

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CAS No.:131105-93-6

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Benzenethiol, 6-Amino-2-Fluoro-3-Methyl- (9Ci) CAS NO 131105-94-7

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CAS No.:131105-94-7

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