Product Name:6-Bromo-4-methyl-2-oxo-2H-chromene-3-carbonitrile

IUPAC Name:6-bromo-4-methyl-2-oxo-2H-chromene-3-carbonitrile

CAS:56394-22-0
Molecular Formula:C11H6BrNO2
Purity:97%
Catalog Number:CM286501
Molecular Weight:264.08

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Product Details

CAS NO:56394-22-0
Molecular Formula:C11H6BrNO2
Melting Point:-
Smiles Code:O=C1OC2=C(C=C(Br)C=C2)C(C)=C1C#N
Density:
Catalog Number:CM286501
Molecular Weight:264.08
Boiling Point:
MDL No:
Storage:

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 Overview 6-Bromo-3-cyano-4-methylcoumarin (6-BCM) is a synthetic compound derived from coumarin and is used in a variety of scientific research applications.
Synthesis Method 6-Bromo-3-cyano-4-methylcoumarin is synthesized from coumarin by a two-step process. In the first step, coumarin is reacted with cyanuric chloride in the presence of a catalyst, such as zinc chloride, to form 3-cyano-4-methylcoumarin. In the second step, 3-cyano-4-methylcoumarin is reacted with bromine to form 6-Bromo-3-cyano-4-methylcoumarin. 
Synthesis and Application 6-Bromo-3-cyano-4-methylcoumarin is widely used in scientific research, particularly in the field of biochemistry. It is used as a fluorescent probe to study the activity of enzymes, as it can be used to detect the presence of enzymes and to measure their activity. 6-Bromo-3-cyano-4-methylcoumarin is also used to study the structure and function of proteins, as it can be used to label proteins and to monitor their activity. Additionally, 6-Bromo-3-cyano-4-methylcoumarin has been used to study the structure and function of nucleic acids, as it can be used to label DNA and to monitor its activity.
Future Directions One possible direction is the use of 6-Bromo-3-cyano-4-methylcoumarin to study the structure and function of proteins and nucleic acids in a variety of biological systems. Additionally, 6-Bromo-3-cyano-4-methylcoumarin could be used to study the activity of enzymes in different cellular environments, such as in the presence of different concentrations of substrates or inhibitors. Finally, 6-Bromo-3-cyano-4-methylcoumarin could be used to study the activity of enzymes in different physiological conditions, such as in the presence of different hormones or in different disease states.