Nom du produit:2-(5-Azetidin-3-yl-1,2,4-oxadiazol-3-yl)pyrimidine hydrochloride

IUPAC Name:2-[5-(azetidin-3-yl)-1,2,4-oxadiazol-3-yl]pyrimidine hydrochloride

CAS:1426290-16-5
Formule moléculaire:C9H10ClN5O
Pureté:97%
Numéro de catalogue:CM534343
Poids moléculaire:239.66

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Détails du produit

N° CAS:1426290-16-5
Formule moléculaire:C9H10ClN5O
Point de fusion:-
Code SMILES:C1(C2=NC=CC=N2)=NOC(C3CNC3)=N1.Cl
Densité:
Numéro de catalogue:CM534343
Poids moléculaire:239.66
Point d'ébullition:
N° Mdl:
Stockage:

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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