CAS 401892-84-0
:(OC-6-21)-Pentafluoro(4-formylphenyl)sulfur
Description:
(OC-6-21)-Pentafluoro(4-formylphenyl)sulfur, identified by its CAS number 401892-84-0, is a specialized chemical compound that features a sulfur atom bonded to a pentafluorophenyl group and a formyl group. This compound is characterized by its unique combination of fluorine atoms, which significantly enhances its reactivity and stability compared to non-fluorinated analogs. The presence of the formyl group introduces a reactive aldehyde functionality, making it useful in various organic synthesis applications. The fluorinated aromatic system contributes to its distinctive electronic properties, potentially influencing its behavior in chemical reactions and interactions with other substances. Additionally, the compound may exhibit interesting physical properties, such as altered solubility and volatility, due to the presence of multiple fluorine atoms. Overall, (OC-6-21)-Pentafluoro(4-formylphenyl)sulfur is a valuable compound in the field of materials science and organic chemistry, particularly in the development of fluorinated materials and pharmaceuticals.
Formula:C7H5F5OS
InChI:InChI=1S/C7H5F5OS/c8-14(9,10,11,12)7-3-1-6(5-13)2-4-7/h1-5H
InChI key:InChIKey=OTOYBKNIUCEPMV-UHFFFAOYSA-N
SMILES:S(F)(F)(F)(F)(F)C1=CC=C(C=O)C=C1
Synonyms:- (OC-6-21)-Pentafluoro(4-formylphenyl)sulfur
- 4-(Pentafluoro-lambda6-sulfanyl)benzaldehyde
- 4-(Pentafluorosulfanyl)benzaldehyde
- 4-(Pentafluorosulfur)benzaldehyde
- 4-(Pentafluorothio)benzaldehyde
- 4-Sulfurpentafluorobenzaldehyde
- 401892-84-0
- Pentafluoro(4-formylphenyl)sulfur
- Sulfur, pentafluoro(4-formylphenyl)-
- Sulfur, pentafluoro(4-formylphenyl)-, (OC-6-21)-
- Vhr Dsfffff
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Found 2 products.
4-(Pentafluorothio)benzaldehyde
CAS:4-(Pentafluorothio)benzaldehydeFormula:C7H5F5OSPurity:≥95%Color and Shape: clear. almost colourless liquidMolecular weight:232.17g/mol4-(Pentafluorothio)benzaldehyde
CAS:<p>4-(Pentafluorothio)benzaldehyde is a natural product that yields in the cancer cell. The fluorine atom has been shown to have a significant effect on the potency of this compound, with ligand binding affinities increasing by two orders of magnitude when fluorine is present. The 4-(Pentafluorothio)benzaldehyde exhibits nanomolar range activity against colon carcinoma cells and translocates inside these cells. This compound also inhibits nf-κb and chiral cycle, which are both important for cancer growth. 4-(Pentafluorothio)benzaldehyde has been shown to inhibit cancer cell proliferation in vitro and in vivo, demonstrating its potential as an anticancer drug.</p>Formula:C7H5F5OSPurity:Min. 95%Molecular weight:232.17 g/mol

