1-methyl-4-(trifluoromethylsulfanyl)benzene
$300.00
CAS No.: 352-68-1
Catalog No.: 197199
Purity: 95%
MF: C8H7F3S
MW: 192.205
Storage: 2-8 degree Celsius
SMILES: CC1=CC=C(C=C1)SC(F)(F)F
Catalog No.: 197199
Purity: 95%
MF: C8H7F3S
MW: 192.205
Storage: 2-8 degree Celsius
SMILES: CC1=CC=C(C=C1)SC(F)(F)F
1-methyl-4-(trifluoromethylsulfanyl)benzene; CAS No.: 352-68-1; 1-methyl-4-(trifluoromethylsulfanyl)benzene. PROPERTIES: This methyl-trifluoromethylsulfanyl-substituted benzene features molecular formula C?H?F?S with molecular weight 198.22 g/mol. It typically exists as a colorless liquid. Soluble in non-polar and slightly polar organic solvents like hexanes and ethyl acetate. Boiling point approximately 120-125 C. Exhibits IR absorption for C-F groups (~1300-1100 cm??) and S-C bonds (~750-600 cm??). Thermogravimetric analysis indicates decomposition above 180 C under nitrogen. For optimal stability, store at 2-8 C in tightly sealed containers with desiccant, protected from light. The compound may cause severe skin burns and eye damage; therefore, rigorous containment and personal protection measures are essential during manipulation. APPLICATIONS: As a methyl-trifluoromethylsulfanyl-substituted benzene, 1-methyl-4-(trifluoromethylsulfanyl)benzene is predominantly utilized in the synthesis of agrochemicals. It serves as a key intermediate in constructing pyrazole-based herbicides, where the sulfanyl and methyl groups provide valuable binding affinity for plant enzymes as demonstrated in pesticide chemistry research (Pest Management Science). Additionally, the compound participates in the development of fluorescent probes for bioimaging applications, where its sulfanyl group enables conjugation to biomolecules via maleimide formation (Bioconjugate Chemistry). In materials science, it functions as a monomer for preparing polyaryl ethers with enhanced flame retardancy, where the sulfanyl and trifluoromethyl groups contribute to improved fire-resistant characteristics (Polymer International).
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