Product Name:1-(1-benzofuran-2-yl)-4,4,4-trifluorobutane-1,3-dione

IUPAC Name:1-(1-benzofuran-2-yl)-4,4,4-trifluorobutane-1,3-dione

CAS:327-24-2
Molecular Formula:C12H7F3O3
Purity:95%+
Catalog Number:CM574092
Molecular Weight:256.18

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Product Details

CAS NO:327-24-2
Molecular Formula:C12H7F3O3
Melting Point:-
Smiles Code:FC(F)(F)C(=O)CC(=O)C1=CC2=CC=CC=C2O1
Density:
Catalog Number:CM574092
Molecular Weight:256.18
Boiling Point:
MDL No:MFCD11523445
Storage:

Category Infos

Fluorinated Compounds
Fluorine is the most electronegative element in the periodic table, and the fluorine atom has a small atomic radius, so fluorine-containing organic compounds have many wonderful properties. For example, the introduction of fluorine atoms or fluorine-containing groups into drug molecules can improve the permeability to cell membranes, metabolic stability and bioavailability; in addition, the introduction of fluorine atoms will improve the lipid solubility of the compound and promote its absorption in the body. The speed of delivery changes the physiological effect. In the field of medicinal chemistry, the introduction of fluorine atoms into organic molecules is an important direction for the development of new anticancer drugs, antitumor drugs, antiviral agents, anti-inflammatory drugs, and central nervous system drugs.
Benzofurans
Benzofuran is an aromatic heterocyclic organic compound with the chemical formula C8H6O. It is a colorless oily liquid at room temperature with an aromatic odor. Benzofuran can be volatilized with water vapor and can be decomposed by potassium permanganate and other oxidants. It is an intermediate for the preparation of amiodarone and indene resin. Benzofuran derivatives are important pharmaceutical intermediates.
Benzofuran | C8H6O | CID 9223 -Chemenu
Benzofuran | C8H6O | CID 9223 |Where to Buy Benzofurans
Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings. This colourless liquid is a component of coal tar.Benzofuran is extracted from coal tar. It is also obtained by dehydrogenation of 2-ethylphenol.

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