Product Name:3-[3-(Trifluoromethyl)phenyl]-5-isoxazolylamine

IUPAC Name:3-[3-(trifluoromethyl)phenyl]-1,2-oxazol-5-amine

CAS:82360-94-9
Molecular Formula:C10H7F3N2O
Purity:97%
Catalog Number:CM190700
Molecular Weight:228.17

Packing Unit Available Stock Price($) Quantity
CM190700-250mg in stock ǧȁ
CM190700-1g in stock țƀț
CM190700-5g in stock ȁNJƙ

For R&D use only.

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Product Details

CAS NO:82360-94-9
Molecular Formula:C10H7F3N2O
Melting Point:-
Smiles Code:NC1=CC(=NO1)C1=CC(=CC=C1)C(F)(F)F
Density:
Catalog Number:CM190700
Molecular Weight:228.17
Boiling Point:
MDL No:MFCD07787059
Storage:Store at 2-8°C.

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.
Isoxazoles
Isoxazole is a liquid heterocyclic compound C3H3NO isomeric with oxazole and having a penetrating odor like that of pyridine. Isoxazoles belong to an important class of five-membered aromatic heterocycles containing two electronegative heteroatoms, nitrogen and oxygen, in a 1,2-relationship and three regular sp2 carbon atoms. These molecules are found to be key components in various synthetic products in daily use and also present as a pharmacophore essential for biological activity in many drugs and bioactive natural products. In addition, isoxazoles have demonstrated their ability to exhibit hydrogen bond donor/acceptor interactions with a variety of enzymes and receptors.

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