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-[1-(Mercaptomethyl)Cyclopropyl]Acetic Acid CAS NO 162515-68-6

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CAS No.:162515-68-6

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Ethyl 3,4,6-Tri-o-Benzyl-1-Thio-Β-D-Galactopyranoside CAS NO 162600-08-0

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CAS No.:162600-08-0

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2-Pyrrolidinone, 1-Acetyl-4-Mercapto-, (S)- (9Ci) CAS NO 162753-53-9

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CAS No.:162753-53-9

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D-Glucose, 2,3,4,5,6-Penta-o-Methyl-, Cyclic (R)-1,1-Binaphthalene-2,2-Diyl Dithioacetal CAS NO 162825-40-3

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CAS No.:162825-40-3

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2-[(2,2,2-Trifluoroethyl)Thio]-Pyridine CAS NO 162965-54-0

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CAS No.:162965-54-0

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3-Iodo-1-Thiophen-2-Yl-Propan-1-Ol CAS NO 164071-58-3

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CAS No.:164071-58-3

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Thiol-Peg-Acid CAS NO 165729-81-7

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CAS No.:165729-81-7

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n-Propyl 3-Mercaptopropionate CAS NO 165804-07-9

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CAS No.:165804-07-9

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