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.

(S)-1-(4-Chlorophenoxy)-3-Mercaptopropan-2-Ol CAS NO 108615-59-4

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CAS No.:108615-59-4

Grade:Pharmacy Grade

Content:99.90%

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Phenyl 2,3,4-Tri-o-Acetyl-1-Thio-Α-L-Rhamnopyranoside CAS NO 108740-74-5

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CAS No.:108740-74-5

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Cyclopentanecarboxylic Acid, 2-Mercapto- (9Ci) CAS NO 108744-13-4

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CAS No.:108744-13-4

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2,3-Bis(Mercaptoacetic Acid)-1,4-Naphthalenedione CAS NO 108900-05-6

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CAS No.:108900-05-6

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2,8-Dinitrodibenzothiophene CAS NO 109041-38-5

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CAS No.:109041-38-5

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Pentanedioic Acid, 2-(Mercaptomethyl)- CAS NO 109333-27-9

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CAS No.:109333-27-9

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2(3H)-Benzothiazolone,4-Nitro-(9Ci) CAS NO 109493-09-6

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CAS No.:109493-09-6

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Content:99.90%

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1-Propen-2-Ol, 1-(4,5-Dihydro-2-Thiazolyl)- (9Ci) CAS NO 109775-43-1

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CAS No.:109775-43-1

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