製品名:7-Hydroxy-4-(trifluoromethyl)coumarin

IUPAC Name:7-hydroxy-4-(trifluoromethyl)-2H-chromen-2-one

CAS番号:575-03-1
分子式:C10H5F3O3
純度:98%
カタログ番号:CM253755
分子量:230.14

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製品詳細

CAS番号:575-03-1
分子式:C10H5F3O3
融点:-
SMILESコード:C1=CC(=CC2=C1C(=CC(O2)=O)C(F)(F)F)O
密度:
カタログ番号:CM253755
分子量:230.14
沸点:311.4°C at 760 mmHg
MDL番号:MFCD00037578
保管方法:Store at room temperature.

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.
Coumarins
Coumarin occurs naturally in a variety of plants, such as lentils, sweet sawdust, vanilla grass, and sweet grass. Coumarin has a simple structure, benzopyrone, associated with different reaction centers. Coumarins are further subdivided into different classes: simple coumarins, pyranocoumarins, furanocoumarins, dicoumarins and isocoumarins. Coumarin derivatives are an important class of natural plant metabolites with various biological activities. They can also be synthesized artificially, and various synthetic coumarin derivatives (azoles, sulfonyls, furans, pyrazoles, etc.) have shown good anticancer, antitumor and antiproliferative activities. Coumarin derivatives are not only effective anticancer agents, but also possess minimum side effects. Based on different substitution patterns, these potential active substances show a great ability to modulate potential anticancer activities.

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