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.

Benzenethiol, 2-Amino-5-Fluoro-3-Methyl- (9Ci) CAS NO 211868-21-2

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CAS No.:211868-21-2

Grade:Pharmacy Grade

Content:99.90%

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Thiazole, 2-Ethynyl-4-Propyl- (9Ci) CAS NO 211940-14-6

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CAS No.:211940-14-6

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Content:99.90%

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(2,4,6-Trimethoxyphenyl)Methanethiol CAS NO 212555-23-2

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CAS No.:212555-23-2

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Content:99.90%

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2-Mercapto-Benzooxazole-4-Carboxylic Acid Methyl Ester CAS NO 213685-54-2

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CAS No.:213685-54-2

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Content:99.90%

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(3-Chloro-2-Fluorophenyl)(Methyl)Sulfane CAS NO 214057-24-6

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CAS No.:214057-24-6

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Content:99.90%

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4-Mercaptoisophthalic Acid CAS NO 214341-16-9

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CAS No.:214341-16-9

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Content:99.90%

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Thiophene-3-Ol, 4-Aminotetrahydro-, 1,1-Dioxide, (3S,4R)- (9Ci) CAS NO 214629-32-0

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CAS No.:214629-32-0

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Content:99.90%

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4-(n-Butylthio)Thioanisole, 98+% CAS NO 216144-37-5

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CAS No.:216144-37-5

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Content:99.90%

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