CAS 4200-06-0
:1-ethynyl-4-(methylsulfanyl)benzene
Description:
1-Ethynyl-4-(methylsulfanyl)benzene, with the CAS number 4200-06-0, is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with an ethynyl group and a methylthio group. The presence of the ethynyl group introduces a triple bond between carbon atoms, contributing to the compound's reactivity and potential applications in organic synthesis. The methylthio group, consisting of a sulfur atom bonded to a methyl group, can influence the compound's electronic properties and solubility. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is generally insoluble in water but soluble in organic solvents, making it useful in various chemical reactions and applications, particularly in the fields of pharmaceuticals and materials science. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C9H8S
InChI:InChI=1/C9H8S/c1-3-8-4-6-9(10-2)7-5-8/h1,4-7H,2H3
SMILES:C#Cc1ccc(cc1)SC
Synonyms:- 1-Ethynyl-4-phenoxybenzene
- 1-Ehynyl-4-phenoxybenzene
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Found 5 products.
1-Ethynyl-4-phenoxybenzene
CAS:Formula:C14H10OPurity:96%Color and Shape:LiquidMolecular weight:194.22861-Ethynyl-4-phenoxybenzene
CAS:Formula:C14H10OPurity:>95.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:194.234′-Phenoxyphenyl acetylene
CAS:Formula:C14H10OPurity:96%Color and Shape:LiquidMolecular weight:194.2331-Ethynyl-4-phenoxybenzene
CAS:<p>1-Ethynyl-4-phenoxybenzene is a monosubstituted chiral compound that is used as an immunosuppressive drug. This drug inhibits the immune response by interfering with the function of T cells and B cells, which are important for antibody production. It also suppresses the production of white blood cells, leading to a decrease in inflammation. 1-Ethynyl-4-phenoxybenzene is orally active and can be taken to reduce inflammation and suppress the immune system. Protonation of this drug leads to its binding to the bacterial enzyme enterobacterial alkaline phosphatase, thereby inhibiting its activity. 1-Ethynyl-4-phenoxybenzene has been shown to inhibit polymerization reactions by acting as a catalyst for reactions involving polyacetylene hydrolysis or polystyrene synthesis.</p>Formula:C14H10OPurity:Min. 95%Color and Shape:Light (Or Pale) Yellow To Brown LiquidMolecular weight:194.23 g/mol




