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235970

Sigma-Aldrich

1,1,1-Trifluoro-2,4-pentanedione

98%

Sinônimo(s):

α,α,α-Trifluoroacetylacetone, 1,1,1-Trifluoroacetylacetone

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About This Item

Fórmula linear:
CH3COCH2COCF3
Número CAS:
367-57-7
Peso molecular:
154.09
Beilstein:
1705177
Número CE:
206-698-5
Número MDL:
MFCD00000427
Código UNSPSC:
12352100
ID de substância PubChem:
24854129
NACRES:
NA.22

Ensaio

98%

forma

liquid

índice de refração

n20/D 1.388 (lit.)

pb

105-107 °C (lit.)

densidade

1.27 g/mL at 25 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CC(=O)CC(=O)C(F)(F)F

InChI

1S/C5H5F3O2/c1-3(9)2-4(10)5(6,7)8/h2H2,1H3

chave InChI

SHXHPUAKLCCLDV-UHFFFAOYSA-N

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Descrição geral

1,1,1-Trifluoro-2,4-pentanedione is known as trifluoro-acetylacetone (TFAA). Molecular structure of 1,1,1-trifluoro-pentane-2,4-dione has been investigated by Density Functional Theory (DFT) calculations.
May darken in storage

Aplicação

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.

Pictogramas

FlameExclamation mark
GHS02,GHS07

Palavra indicadora

Warning

Frases de perigo

H226,H302 + H312 + H332

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 3

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

78.8 °F - closed cup

Ponto de fulgor (°C)

26 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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M Y Khuhawar et al.
Journal of chromatography. B, Biomedical sciences and applications, 723(1-2), 17-24 (1999-03-18)
Trifluoroacetylacetone (FAA) derivatives of 1,4-diaminobutane (putrescine) (Pu) and 1,5-diaminopentane (cadaverine) (CA) were prepared and characterized by elemental microanalysis, IR, and mass spectrometry. Diamine derivatives were eluted from capillary gas chromatographic (CGC) column BP1 (12 m x 0.22 mm I.D.) or
Belén Zarranz et al.
Bioorganic & medicinal chemistry, 12(13), 3711-3721 (2004-06-10)
As a continuation of our research in quinoxaline 1,4-di-N-oxide and with the aim of obtaining new anticancer agents, which can improve the current chemotherapeutic treatments, new series of 2-alkylcarbonyl and 2-benzoyl-3-trifluoromethylquinoxaline 1,4-di-N-oxide derivatives have been synthesized and evaluated for in
Analysis of aluminium in tablets by derivative ultraviolet spectrophotometry.
L Nobile et al.
Die Pharmazie, 46(2), 138-139 (1991-02-01)
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