Название продукции:6-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-chromen-2-one

IUPAC Name:6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-chromen-2-one

CAS:1408287-07-9
Молекулярная формула:C15H17BO4
Чистота:95%
Номер в каталоге:CM208960
Молекулярная масса:272.11

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Информация о продукции

Номер CAS:1408287-07-9
Молекулярная формула:C15H17BO4
Точка плавления:-
Smiles-код:O=C1C=CC2=C(O1)C=CC(B3OC(C)(C)C(C)(C)O3)=C2
Плотность:
Номер в каталоге:CM208960
Молекулярная масса:272.11
Точка кипения:
Номер Mdl:MFCD27936531
Хранение:

Category Infos

Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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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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