Nom du produit:tert-Butyl 3-((1-(pyrimidin-2-yl)pyrrolidin-3-yl)carbamoyl)azetidine-1-carboxylate

IUPAC Name:tert-butyl 3-{[1-(pyrimidin-2-yl)pyrrolidin-3-yl]carbamoyl}azetidine-1-carboxylate

CAS:1956356-07-2
Formule moléculaire:C17H25N5O3
Pureté:95%
Numéro de catalogue:CM284901
Poids moléculaire:347.42

Unité d'emballage Stock disponible Prix($) Quantité
CM284901-1g in stock ƏŔŭ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:1956356-07-2
Formule moléculaire:C17H25N5O3
Point de fusion:-
Code SMILES:O=C(N1CC(C(NC2CN(C3=NC=CC=N3)CC2)=O)C1)OC(C)(C)C
Densité:
Numéro de catalogue:CM284901
Poids moléculaire:347.42
Point d'ébullition:
N° Mdl:MFCD28991820
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.
Pyrrolidines
Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase 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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