Название продукции:N-[(2-phenyl-1,3-thiazol-4-yl)methyl]-1-(6-phenylpyrimidin-4-yl)azetidine-3-carboxamide
IUPAC Name:N-[(2-phenyl-1,3-thiazol-4-yl)methyl]-1-(6-phenylpyrimidin-4-yl)azetidine-3-carboxamide
- CAS:2034257-96-8
- Молекулярная формула:C24H21N5OS
- Чистота:95%+
- Номер в каталоге:CM969949
- Молекулярная масса:427.53
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Информация о продукции
- Номер CAS:2034257-96-8
- Молекулярная формула:C24H21N5OS
- Точка плавления:-
- Smiles-код:O=C(NCC1=CSC(=N1)C1=CC=CC=C1)C1CN(C1)C1=CC(=NC=N1)C1=CC=CC=C1
- Плотность:
- Номер в каталоге:CM969949
- Молекулярная масса:427.53
- Точка кипения:
- Номер Mdl:
- Хранение:
Category Infos
- Thiazoles
- Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.
- 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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