Trifluoroacetaldehyde hydrate, tech., ca 75% in water, Thermo Scientific Chemicals
Trifluoroacetaldehyde hydrate, tech., ca 75% in water, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Trifluoroacetaldehyde hydrate, tech., ca 75% in water, Thermo Scientific Chemicals

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10 g
50 g
Catalog number A13234.09
also known as A13234-09
Price (USD)/ Each
106.00
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Quantity:
10 g
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Trifluoroacetaldehyde hydrate, tech., ca 75% in water, Thermo Scientific Chemicals
Catalog numberA13234.09
Price (USD)/ Each
106.00
-
Add to cart
Chemical Identifiers
CAS421-53-4
IUPAC Name2,2,2-trifluoroacetaldehyde
Molecular FormulaC2HF3O
InChI KeyJVTSHOJDBRTPHD-UHFFFAOYSA-N
SMILESFC(F)(F)C=O
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SpecificationsSpecification SheetSpecification Sheet
Assay (Aqueous acid-base Titration)70 - 80%
Refractive Index1.3375 - 1.3415 @20?C
Formliquid
CommentHydrate reacts with KF reagent as well as free water
Water Content (Karl Fischer Titration)ca. 41 - 32%
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One general application of trifluoroacetaldehyde is the preparation of trifluoroethylamino derivatives via reductive amination reaction. This synthesis includes the formation of the corresponding N,O-acetal intermediates followed by their reduction using NaBH4 or 2-picoline borane complex, affording the target trifluoroethylamino compounds in moderate to good yields. Another general application of trifluoroacetaldehyde is the synthesis of chiral α-substituted trifluoroethylamino compounds.

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
One general application of trifluoroacetaldehyde is the preparation of trifluoroethylamino derivatives via reductive amination reaction. This synthesis includes the formation of the corresponding N,O-acetal intermediates followed by their reduction using NaBH4 or 2-picoline borane complex, affording the target trifluoroethylamino compounds in moderate to good yields. Another general application of trifluoroacetaldehyde is the synthesis of chiral α-substituted trifluoroethylamino compounds.

Solubility
Soluble in water.

Notes
Store at room temperature. Incompatible with oxidizing agents. Keep in cool place.
RUO – Research Use Only

General References:

  1. G. K. Surya Prakash.; Zhe Zhang.; Fang Wang.; Socrates Munoz.; George A. Olah. Nucleophilic Trifluoromethylation of Carbonyl Compounds: Trifluoroacetaldehyde Hydrate as a Trifluoromethyl Source.J. Org. Chem. 2013, 78 (7),3300-3305 .
  2. Mauno M. Airaksinen.; Per H. Rosenberg.; Tapani Tammisto. A Possible Mechanism of Toxicity of Trifluoroethanol and Other Halothane Metabolites.Acta Pharmacologica et Toxicologica. 1970, 28 (4),299-304 .