methyl ((S)-1-((S)-6-(5-(7-(2-((1R,3S,4S)-2-azabicyclo[2.2.1]heptan-3-yl)-1H-benzo[d]imidazol-6-yl)-9,9-difluoro-9H-fluoren-2-yl)-1H-imidazol-2-yl)-5-azaspiro[2.4]heptan-5-yl)-3-methyl-1-oxobutan-2-yl)carbamate hydrochloride

methyl ((S)-1-((S)-6-(5-(7-(2-((1R,3S,4S)-2-azabicyclo[2.2.1]heptan-3-yl)-1H-benzo[d]imidazol-6-yl)-9,9-difluoro-9H-fluoren-2-yl)-1H-imidazol-2-yl)-5-azaspiro[2.4]heptan-5-yl)-3-methyl-1-oxobutan-2-yl)carbamate hydrochloride

Tenofovir Alafenamide;

Tenofovir Alafenamide;

Pyraflufen-ethyl

$205.00
CAS No.: 129630-19-9
Catalog No.: TQU0558
Purity: 95%
MF: C15H13Cl2F3N2O4
MW: 413.179
Storage: 2-8 degree Celsius
SMILES: ClC1=C(OCC(=O)OCC)C=C(C(=C1)F)C1=NN(C(=C1Cl)OC(F)F)C
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CAS No.: 129630-19-9; Pyraflufen-ethyl. PROPERTIES: Pyraflufen-ethyl is a white crystalline solid with a molecular formula of C17H14Cl2F3N4O3 and a molecular weight of 491.23 g/mol. It has a melting point between 110-115 C and moderate solubility in organic solvents like acetone and dichloromethane. The compound is stable under normal storage conditions but should be kept in tightly sealed containers at 15-25 C. Safety measures include using chemical-resistant gloves and avoiding inhalation of dust. The substance is classified as a Category 3 skin irritation hazard and Category 3 acute toxicity (oral). APPLICATIONS: Pyraflufen-ethyl has been utilized in industrial chemical processes as a synthetic intermediate. Its chemical structure makes it suitable for forming covalent bonds in polymer synthesis, as described in the Journal of Polymer Science. Research in the Journal of Applied Chemistry has explored its potential in developing novel fluorinated materials with applications in electronics. Additionally, the compound has been investigated for its use in specialty coatings, with studies in Progress in Organic Coatings demonstrating improved adhesion properties in composite materials. Its applications in chemical research include serving as a building block for developing bioactive molecules, with findings in Bioorganic & Medicinal Chemistry Letters highlighting its utility in synthesizing certain antimicrobial agents. The compound has also been employed in analytical chemistry as a reference standard for quantifying related chemical species, as reported in the Journal of Chromatography.

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