Название продукции:5-methyl-N-(2-{[3-(thiophen-2-yl)-1,2,4-oxadiazol-5-yl]methyl}phenyl)-1,2-oxazole-4-carboxamide

IUPAC Name:5-methyl-N-(2-{[3-(thiophen-2-yl)-1,2,4-oxadiazol-5-yl]methyl}phenyl)-1,2-oxazole-4-carboxamide

CAS:1705278-15-4
Молекулярная формула:C18H14N4O3S
Чистота:95%+
Номер в каталоге:CM895624
Молекулярная масса:366.4

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Информация о продукции

Номер CAS:1705278-15-4
Молекулярная формула:C18H14N4O3S
Точка плавления:-
Smiles-код:CC1=C(C=NO1)C(=O)NC1=C(CC2=NC(=NO2)C2=CC=CS2)C=CC=C1
Плотность:
Номер в каталоге:CM895624
Молекулярная масса:366.4
Точка кипения:
Номер Mdl:
Хранение:

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
Oxadiazoles
Oxadiazoles are a class of heterocyclic aromatic compounds with the molecular formula C2H2N2O, which have special biological activities and thermodynamic properties. Five-membered heterocyclic moieties composed of three or two heteroatoms are of great interest to researchers because these compounds show significant therapeutic potential. These heterocycles can serve as a building block for the development of novel molecular structures.
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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