2,6-Bis(trifluoromethyl)benzoic acid, 98%
2,6-Bis(trifluoromethyl)benzoic acid, 98%
2,6-Bis(trifluoromethyl)benzoic acid, 98%
Thermo Scientific Chemicals

2,6-Bis(trifluoromethyl)benzoic acid, 98%

CAS: 24821-22-5 | C9H4F6O2 | 258.119 g/mol
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Quantity:
1 g
5 g
Catalog number B20486.03
also known as B20486-03
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Quantity:
1 g
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Chemical Identifiers
CAS24821-22-5
IUPAC Name2,6-bis(trifluoromethyl)benzoic acid
Molecular FormulaC9H4F6O2
InChI KeyXZNLSDPNMNWCRE-UHFFFAOYSA-N
SMILESOC(=O)C1=C(C=CC=C1C(F)(F)F)C(F)(F)F
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale cream to pale yellow
FormCrystals or powder or crystalline powder
Melting Point (clear melt)134.0-140.0?C
Assay (Silylated GC)≥97.5%
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
2,6-Bis(trifluoromethyl)benzoic acid is used as an organic intermediate in synthesis. It is also used as a pharmaceutical intermediate and organic intermediate in chemical 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
2,6-Bis(trifluoromethyl)benzoic acid is used as an organic intermediate in synthesis. It is also used as a pharmaceutical intermediate and organic intermediate in chemical synthesis.

Solubility
Soluble in water.

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

General References:

  1. H Wingert.; G Maas.; M Regitz. Syntheses with cyclobutadienes -151. Prismane / dewar benzene isomerization- x-ray crystal structure of tert-butyl 3,4,5-tri-tert-butyl-2,6-bis(trifluoromethyl)prismane-1-carboxylate. The Tetrahedron. 198642 ( 19), 5341-5353.
  2. HA Chiong.; QN Pham.; O Daugulis. Two methods for direct ortho-arylation of benzoic acids. J. Am. Chem. Soc. 2007129 ( 32), 9879-9884.