製品名: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番号:438035-77-9
- 分子式:C16H19ClO3
- 純度:97%
- カタログ番号:CM286760
- 分子量:294.78
包装単位 |
有効在庫 |
価格(USD) |
数量 |
CM286760-1g |
in stock |
-- |
|
|
|
製品詳細
- CAS番号:438035-77-9
- 分子式:C16H19ClO3
- 融点:-
- SMILESコード:O=C1C(CCCCCC)=C(C)C2=C(O1)C=C(O)C(Cl)=C2
- 密度:
- カタログ番号:CM286760
- 分子量:294.78
- 沸点:
- MDL番号:MFCD03029475
- 保管方法:
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.
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.
|