Product Name:2-(5-{1-[(E)-2-(4-methylphenyl)ethenesulfonyl]azetidin-3-yl}-1,2,4-oxadiazol-3-yl)pyrimidine

IUPAC Name:2-(5-{1-[(1E)-2-(4-methylphenyl)ethenesulfonyl]azetidin-3-yl}-1,2,4-oxadiazol-3-yl)pyrimidine

CAS:1331426-64-2
Molecular Formula:C18H17N5O3S
Purity:95%+
Catalog Number:CM817971
Molecular Weight:383.43

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Product Details

CAS NO:1331426-64-2
Molecular Formula:C18H17N5O3S
Melting Point:-
Smiles Code:CC1=CC=C(\C=C\S(=O)(=O)N2CC(C2)C2=NC(=NO2)C2=NC=CC=N2)C=C1
Density:
Catalog Number:CM817971
Molecular Weight:383.43
Boiling Point:
MDL No:
Storage:

Category Infos

Pyrimidines
Pyrimidine, also known as 1,3-diazobenzene, is a heterocyclic compound with the chemical formula C4H4N2. Pyrimidine is formed by substituting 2 nitrogen atoms for 2 carbons in the meta-position of benzene. It is a diazine and retains its aromaticity. Derivatives of pyrimidine widely exist in organic macromolecular nucleic acids, and many drugs also contain pyrimidine rings. In nucleic acids, three nucleobases are pyrimidine derivatives: cytosine, thymine and uracil. There are a variety of pyrimidine-containing drugs on the market, most of which are kinase inhibitors.
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.
Azetidines
Azetidines are an important class of saturated four-membered nitrogen-containing heterocyclic compounds. The research hotspots related to this structure mainly focus on two aspects: one is the research of pharmaceutical chemistry; the other is related to chiral azetidines, using rigid azetidine compounds as chiral ligands for asymmetric catalytic reactions. Many nitrogen-containing heterocycles play important roles in drug structures, and in many cases small structural changes can improve ligand selectivity and pharmacokinetic properties.
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