Название продукции:7-(Diethylamino)-4-methyl-3-(morpholinomethyl)-2H-chromen-2-one

IUPAC Name:7-(diethylamino)-4-methyl-3-[(morpholin-4-yl)methyl]-2H-chromen-2-one

CAS:142878-43-1
Молекулярная формула:C19H26N2O3
Чистота:97%
Номер в каталоге:CM291609
Молекулярная масса:330.43

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Информация о продукции

Номер CAS:142878-43-1
Молекулярная формула:C19H26N2O3
Точка плавления:-
Smiles-код:O=C1C(CN2CCOCC2)=C(C)C3=C(O1)C=C(N(CC)CC)C=C3
Плотность:
Номер в каталоге:CM291609
Молекулярная масса:330.43
Точка кипения:
Номер Mdl:MFCD00232961
Хранение:

Category Infos

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.
morpholine price
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Coumarins
Coumarin occurs naturally in a variety of plants, such as lentils, sweet sawdust, vanilla grass, and sweet grass. Coumarin has a simple structure, benzopyrone, associated with different reaction centers. Coumarins are further subdivided into different classes: simple coumarins, pyranocoumarins, furanocoumarins, dicoumarins and isocoumarins. Coumarin derivatives are an important class of natural plant metabolites with various biological activities. They can also be synthesized artificially, and various synthetic coumarin derivatives (azoles, sulfonyls, furans, pyrazoles, etc.) have shown good anticancer, antitumor and antiproliferative activities. Coumarin derivatives are not only effective anticancer agents, but also possess minimum side effects. Based on different substitution patterns, these potential active substances show a great ability to modulate potential anticancer activities.

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