
CAS 4001-61-0: 2,5-Dimethylbenzenethiol
Formula:C8H10S
InChI:InChI=1S/C8H10S/c1-6-3-4-7(2)8(9)5-6/h3-5,9H,1-2H3
InChI key:InChIKey=NHAUBUMQRJWWAT-UHFFFAOYSA-N
SMILES:SC1=C(C)C=CC(C)=C1
Synonyms:- 2,5-dimethylbenzenethiolate
- 2,5-Dimethylbenzene-1-thiol
- 2,5-Dimethylthiophenol
- 2,5-Dimethylbenzenethiol
- 2,5-Dimethylbenzenethiol
- 2,5-Xylenethiol
- Benzenethiol, 2,5-dimethyl-
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Found 8 products.
2,5-Dimethylthiophenol
CAS:Purity:98.0%Color and Shape:Liquid, Clear colourless liquidMolecular weight:138.22999572753906Vortioxetine Impurity 42
CAS:Formula:C8H10SColor and Shape:White To Off-White SolidMolecular weight:138.232,5-Dimethylbenzenethiol
CAS:Formula:C8H10SPurity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:138.232,5-Dimethylthiophenol
CAS:2,5-DimethylthiophenolFormula:C8H10SPurity:95%Color and Shape: clear. colourless liquidMolecular weight:138.23g/mol2,5-Dimethylbenzenethiol
CAS:2,5-Dimethylbenzenethiol is a functionalized thiol that is used in cross-coupling reactions. It can be used to synthesize organic compounds with a wide range of structures, including alcohols, amines, carbonyls, and esters. In addition to being an efficient method for the synthesis of these compounds, this thiol has been shown to be cytotoxic against cancer cells. 2,5-Dimethylbenzenethiol has also been shown to have gas sensing properties. The synthesis of this thiol is achieved through a reaction between 2-bromobenzene and ethanethiol. This reaction produces 2-bromoethanethiol and 2,5-dimethylbenzenethiol as products. This molecule then undergoes hydrolysis in order to produce the final product. The molecular structure of this compound consists of two benzene rings connected by a carbon chain with two methyl groups on either end of theFormula:C8H10SPurity:Min. 95%Molecular weight:138.23 g/mol