Sodium trifluoroacetate, 98%

Name: Sodium trifluoroacetate, 98%
SKU: A14613.36

CAS: 2923-18-4 | C2F3NaO2 | 136.01 g/mol

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数量:

25 g

100 g

500 g

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製品番号（カタログ番号） A14613.36

または、製品番号A14613-36

価格（JPY）

数量:

500 g

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化学物質識別子

CAS2923-18-4

IUPAC Namesodium trifluoroacetate

Molecular FormulaC2F3NaO2

InChI KeyUYCAUPASBSROMS-UHFFFAOYSA-M

SMILES[Na+].[O-]C(=O)C(F)(F)F

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仕様

スペックシート

Appearance (Color)White

Identification (FTIR)Conforms

FormCrystals or powder or crystalline powder or lumps

Assay (Non-aqueous acid-base Titration)≥97.5 to ≤102.5%

Sodium trifluoroacetate is used in acid catalyzed reactions. It is also used as an intermediate for active pharmaceutical ingredients (API). Further, it acts as a precursor for the trifluoromethylation of aldehydes using copper(I) halide as a catalyst.

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
Sodium trifluoroacetate is used in acid catalyzed reactions. It is also used as an intermediate for active pharmaceutical ingredients (API). Further, it acts as a precursor for the trifluoromethylation of aldehydes using copper(I) halide as a catalyst.

Solubility
Soluble in water.

Notes
Incompatible with strong oxidizing agents and strong bases. Hygroscopic. Moisture sensitive.

RUO – Research Use Only

General References:

Carbene precursor, compare Sodium chlorodifluoroacetate, A15756.
In the presence of CuI, converts aryl iodides to benzotrifluorides: Chem. Lett., 1719 (1981); J. Chem. Soc., Perkin 1, 921 (1988).
Chan, K. S. L.; Fu, H. Y.; Yu, J. Q. Palladium(II)-Catalyzed Highly Enantioselective C-H Arylation of Cyclopropylmethylamines. J. Am. Chem. Soc. 2015, 137 (5), 2042-2046.
Castano, M.; Seo, K. S.; Guo, K.; Becker, M. L.; Wesdemiotis, C.; Puskas, J. E. Green polymer chemistry: synthesis of symmetric and asymmetric telechelic ethylene glycol oligomers. Polym. Chem. 2015, 6 (7), 1137-1142.