Название продукции:azetidin-3-one hydrochloride

IUPAC Name:azetidin-3-one hydrochloride

CAS:17557-84-5
Молекулярная формула:C3H6ClNO
Чистота:95%+
Номер в каталоге:CM103679
Молекулярная масса:107.54

Упаковочная единица Доступно для заказа Цена ($) Количество
CM103679-25g in stock ɅNJ
CM103679-100g in stock țNJŴ

Только для использования в НИОКР..

Форма запроса

   refresh    

Информация о продукции

Номер CAS:17557-84-5
Молекулярная формула:C3H6ClNO
Точка плавления:-
Smiles-код:Cl.O=C1CNC1
Плотность:
Номер в каталоге:CM103679
Молекулярная масса:107.54
Точка кипения:
Номер Mdl:MFCD01861742
Хранение:

Category Infos

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.
Where to buy Azetidines
Where to buy ADC-Cytotoxins? Chemenu Provide Azetidines with high quality and competitive price. Contact us Now.

Column Infos

Alicyclic Heterocycles
When the ends of the chains are joined together into a ring, cyclic compounds result; such substances often are referred to as carbocyclic or alicyclic compounds. Substitution of one or more of the ring carbon atoms in the molecules of a carbocyclic compound with a heteroatom gives a heterocyclic compound.
Palazestrant
Olema Oncology is advancing the development of Palazestrant (OP-1250) in metastatic breast cancer in 2024. Palazestrant is an oral complete ER antagonist (CERAN) and selective ER degrader (SERD). It potently binds and completely blocks transcriptional activity of both wild-type and ESR1-mutant ER with favorable tolerability and anti-tumor activity.
Palazestrant is under clinical development both in combination with Novartis' CDK4/6 inhibitor Kisqali (Ribociclib) as a first-line therapy for advanced estrogen receptor-positive, HER2-negative breast cancer, and as a monotherapy compared to standard of care treatment in second- and third-line advanced or metastatic ER-positive, HER2-negative breast cancer.