Название продукции: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
- Молекулярная формула:C17H25N5O3
- Чистота:95%
- Номер в каталоге:CM284901
- Молекулярная масса:347.42
Только для использования в НИОКР..
Информация о продукции
- Номер CAS:1956356-07-2
- Молекулярная формула:C17H25N5O3
- Точка плавления:-
- Smiles-код:O=C(N1CC(C(NC2CN(C3=NC=CC=N3)CC2)=O)C1)OC(C)(C)C
- Плотность:
- Номер в каталоге:CM284901
- Молекулярная масса:347.42
- Точка кипения:
- Номер Mdl:MFCD28991820
- Хранение:
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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