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1,1,1-Trifluoro-2,4-pentanedione, 98%, Thermo Scientific Chemicals
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Catalog number A14682.06
also known as A14682-06
Price (USD)/ Each
29.80
-
Quantity:
5 g
Price (USD)/ Each
29.80
1,1,1-Trifluoro-2,4-pentanedione, 98%, Thermo Scientific Chemicals
Catalog numberA14682.06
Price (USD)/ Each
29.80
-
Chemical Identifiers
CAS367-57-7
Specifications
Specification Sheet
Specification SheetFormLiquid
Refractive Index1.3855-1.3900 @ 20?C
Appearance (Color)Clear colorless to yellow
CommentMaterial sourced in UK and US
Assay (GC)≥97.5% (sum of tautomers)
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1,1,1-Trifluoro-2,4-pentanedione has been used as reagent in the preparation of 2-alkylcarbonyl and 2-benzoyl-3-trifluoromethylquinoxaline 1,4-di-N-oxide derivatives.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1,1,1-Trifluoro-2,4-pentanedione has been used as reagent in the preparation of 2-alkylcarbonyl and 2-benzoyl-3-trifluoromethylquinoxaline 1,4-di-N-oxide derivatives.
Solubility
Soluble in water (slightly) and many organic solvents.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
1,1,1-Trifluoro-2,4-pentanedione has been used as reagent in the preparation of 2-alkylcarbonyl and 2-benzoyl-3-trifluoromethylquinoxaline 1,4-di-N-oxide derivatives.
Solubility
Soluble in water (slightly) and many organic solvents.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Belen Zarranz; Andres Jaso; Ignacio Aldana; Antonio Monge. Synthesis and anticancer activity evaluation of new 2-alkylcarbonyl and 2-benzoyl-3-trifluoromethyl-quinoxaline 1,4-di-N-oxide derivatives. Bioorganic & Medicinal Chemistry. 2004, 12, (13),3711-3721
- Mansoureh Zahedi-Tabrizi; Fariba Tayyari; Zainab Moosavi-Tekyeh; Alireza Jalali; Sayyed Faramarz Tayyari. Structure and vibrational assignment of the enol form of 1,1,1-trifluoro-2,4-pentanedione. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2006, 65, (2),387-396
- Chelating ligand. Review of chemistry of fluorinated ß-diketones: Russ. Chem. Rev., 50, 180 (1981).
- For use in the preparation of trifluoromethyl pyrimidines by reaction with guanidines, see: Synth. Commun., 20, 913 (1990):