Product Name:2-(4-(Azetidin-3-yl)piperazin-1-yl)pyrimidine dihydrochloride

IUPAC Name:2-[4-(azetidin-3-yl)piperazin-1-yl]pyrimidine dihydrochloride

CAS:1956322-44-3
Molecular Formula:C11H19Cl2N5
Purity:95%
Catalog Number:CM284876
Molecular Weight:292.21

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Product Details

CAS NO:1956322-44-3
Molecular Formula:C11H19Cl2N5
Melting Point:-
Smiles Code:[H]Cl.[H]Cl.C1(N2CCN(C3CNC3)CC2)=NC=CC=N1
Density:
Catalog Number:CM284876
Molecular Weight:292.21
Boiling Point:
MDL No:MFCD28991714
Storage:

Category Infos

Piperazines
Piperazine is an organic compound consisting of a six-membered ring containing two nitrogen atoms in opposite positions in the ring. The chemical formula of piperazine is C4H10N2, and it is an important pharmaceutical intermediate. Pyrimidines and piperazines are known to be the backbone of many bulk compounds and important core structures for approved drugs; studies have shown that combining a pyridine ring with a piperazine moiety within a single structural framework enhances biological activity.
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.
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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