Название продукции:6-Chloro-3-hexyl-7-hydroxy-4-methyl-2H-chromen-2-one

IUPAC Name:6-chloro-3-hexyl-7-hydroxy-4-methyl-2H-chromen-2-one

CAS:438035-77-9
Молекулярная формула:C16H19ClO3
Чистота:97%
Номер в каталоге:CM286760
Молекулярная масса:294.78

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Информация о продукции

Номер CAS:438035-77-9
Молекулярная формула:C16H19ClO3
Точка плавления:-
Smiles-код:O=C1C(CCCCCC)=C(C)C2=C(O1)C=C(O)C(Cl)=C2
Плотность:
Номер в каталоге:CM286760
Молекулярная масса:294.78
Точка кипения:
Номер Mdl:MFCD03029475
Хранение:

Category Infos

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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Product Other Information

Product Overview 6-Chloro-3-hexyl-7-hydroxy-4-methyl-2H-chromen-2-one (438035-77-9) is a naturally occurring chromenone that has been used in a variety of scientific research applications.
Chemical Properties 6-Chloro-3-hexyl-7-hydroxy-4-methyl-2H-chromen-2-one (438035-77-9) is relatively stable and can be stored for extended periods of time without significant degradation.
Synthesis and Application 6-Chloro-3-hexyl-7-hydroxy-4-methyl-2H-chromen-2-one (438035-77-9) has been studied extensively due to its unique properties, which make it an attractive target for research. It has been used as a model compound for studying the structure and function of chromenones, as well as for investigating their potential applications in medicine, agriculture, and biotechnology. Additionally, it has been studied for its potential use in the synthesis of other compounds, such as the anticancer agent imatinib.