3-Benzoyl-1,1,1-trifluoroacetone, 98+%
3-Benzoyl-1,1,1-trifluoroacetone, 98+%
3-Benzoyl-1,1,1-trifluoroacetone, 98+%
Thermo Scientific Chemicals

3-Benzoyl-1,1,1-trifluoroacetone, 98+%

CAS: 326-06-7 | C10H7F3O2 | 216.16 g/mol
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25 g
100 g
Catalog number A17110.14
also known as A17110-14
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Quantity:
25 g
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Price (USD)
51.65
Online Exclusive
56.80
Save 5.15 (9%)
Each
Chemical Identifiers
CAS326-06-7
SpecificationsSpecification SheetSpecification Sheet
Assay (GC)>98.0%
CommentProduct may contain a small amount of particulate matter from the manufacturing process.
Appearance (Color)White to cream or pale yellow
FormCrystalline solid
3-Benzoyl-1,1,1-trifluoroacetone, is used as a primary and secondary intermediate. It is used as an Intermediate in organic synthesis.

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
3-Benzoyl-1,1,1-trifluoroacetone, is used as a primary and secondary intermediate. It is used as an Intermediate in organic synthesis.

Solubility
Sparingly Soluble in water (0.24 g/L) (25°C).

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from oxidizing agents.
RUO – Research Use Only

General References:

  1. H Yokoi. The new triplet-state dimers formed by mixing bis(n-alkylsalicylaldiminato)copper(ii) with certain bis (β-diketonato) copper(ii) complexes in toluene. Chemistry letters. 19702 (9), 1023-1026.
  2. VO Iaroshenko.; D Ostrovskyi.; K Ayub. Synthesis of 4-Trifluoromethylpyridines by [5+ 1] Cyclization of 3-Hydroxy-pent-4-yn-1-ones with Urea. Advanced Synthesis and catalysis. 2013355 (2-3), 576-588.
  3. Chelating ligand.