Nom du produit:5-(azetidin-1-yl)-2-(piperidin-3-yl)-2,3-dihydropyridazin-3-one
IUPAC Name:5-(azetidin-1-yl)-2-(piperidin-3-yl)-2,3-dihydropyridazin-3-one
- CAS：1803587-53-2
- Formule moléculaire：C12H18N4O
- Pureté：95%+
- Numéro de catalogue：CM412992
- Poids moléculaire：234.3
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1803587-53-2
- Formule moléculaire:C12H18N4O
- Point de fusion:-
- Code SMILES:O=C1C=C(C=NN1C1CCCNC1)N1CCC1
- Densité:
- Numéro de catalogue:CM412992
- Poids moléculaire:234.3
- Point d'ébullition:
- N° Mdl:MFCD28246223
- Stockage:
Category Infos
- Pyridazines
- Pyridazine, also known as o-diazobenzene, is a six-membered heterocyclic compound containing two nitrogen heteroatoms in the 1 and 2 positions with a special structure and a wide biological activity. Pyridazine is more and more popular in drug development, and a variety of pyridazine drugs have been developed and marketed. From the perspective of the therapeutic field, pyridazine drug molecules are mainly used for tumor treatment, but also involve in many therapeutic fields such as inflammation, hypertension and cardiovascular disease. With the increase and in-depth of research, pyridazine drugs will play more roles in the treatment of diseases.
- Piperidines
- Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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- 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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