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.

2-Mercaptopropionaldehyde CAS NO 54354-14-2

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CAS No.:54354-14-2

Grade:Pharmacy Grade

Content:99.90%

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2-Bromo-4-Chlorobenzenethiol CAS NO 54404-01-2

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CAS No.:54404-01-2

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3,4-Dimethoxybenzyl Mercaptan CAS NO 54810-59-2

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CAS No.:54810-59-2

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Ethyl 2-Mercaptocyclohex-1-Enecarboxylate CAS NO 54928-91-5

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CAS No.:54928-91-5

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3-((2-Mercapto-1-Methylpropyl)Thio)-2-Butanol CAS NO 54957-02-7

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CAS No.:54957-02-7

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2,3-Dihydro-1H-Inden-5-Yl Hydrosulfide CAS NO 55119-14-7

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CAS No.:55119-14-7

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3-Butyltetrahydro-2-Methylthiophene CAS NO 55320-22-4

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CAS No.:55320-22-4

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2-Bromo-5-Fluorobenzenethiol CAS NO 55389-14-5

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CAS No.:55389-14-5

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