Название продукции:4-(2-Chloro-6-((4-methylpiperazin-1-yl)methyl)-thieno[3,2-d]pyrimidin-4-yl)morpholine

IUPAC Name:4-{2-chloro-6-[(4-methylpiperazin-1-yl)methyl]thieno[3,2-d]pyrimidin-4-yl}morpholine

CAS:885618-54-2
Молекулярная формула:C16H22ClN5OS
Чистота:95%
Номер в каталоге:CM151488
Молекулярная масса:367.9

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Информация о продукции

Номер CAS:885618-54-2
Молекулярная формула:C16H22ClN5OS
Точка плавления:-
Smiles-код:CN1CCN(CC2=CC3=NC(Cl)=NC(N4CCOCC4)=C3S2)CC1
Плотность:
Номер в каталоге:CM151488
Молекулярная масса:367.9
Точка кипения:
Номер Mdl:MFCD22690814
Хранение:

Category Infos

Piperazines
Piperazine is an organic compound consisting of a six-membered ring containing two nitrogen atoms in opposite positions in the ring. The chemical formula of piperazine is C4H10N2, and it is an important pharmaceutical intermediate. Pyrimidines and piperazines are known to be the backbone of many bulk compounds and important core structures for approved drugs; studies have shown that combining a pyridine ring with a piperazine moiety within a single structural framework enhances biological activity.
Morpholines
Morpholine contains secondary amine groups and has all the typical reactive characteristics of secondary amine groups. It can react with inorganic acids to form salts, and react with organic acids to form salts or amides, which can be subjected to alkylation reaction, and can also be reacted with ethylene oxide, ketone or Willgerodt reaction. Morpholine is a six-membered ring containing oxygen and nitrogen, and its alkalinity is much lower than that of its parent piperidine. The marketed morpholine drugs are mainly distributed in the fields of tumors, cardiovascular and cerebrovascular diseases, respiratory system diseases, digestive system diseases, infectious diseases and mental disorders.
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Thienopyrimidines
Thienopyrimidines are a class of heterocyclic compounds with diverse biological activities depending on their detailed substitution patterns. In addition, many thienopyrimidine derivatives have shown potent activity against cancer cell lines and specific oncogenes.

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