4H-1-Benzopyran-4-one, 3-bromo-7-methoxy-


Chemical Name: 4H-1-Benzopyran-4-one, 3-bromo-7-methoxy-
CAS Number: 73220-41-4
Product Number: AG005Q0A(AGN-PC-01X5HT)
Synonyms:
MDL No:
Molecular Formula: C10H7BrO3
Molecular Weight: 255.0648

Identification/Properties


Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
255.067g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
253.958g/mol
Monoisotopic Mass:
253.958g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
275
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



3-Bromo-7-methoxy-4H-chromen-4-one is a versatile compound that finds wide applications in chemical synthesis. This compound is commonly used as a key intermediate in the synthesis of various biologically active molecules and pharmaceuticals. Its unique structure allows for the introduction of different functional groups, making it a valuable building block in organic chemistry.One of the primary applications of 3-Bromo-7-methoxy-4H-chromen-4-one is in the synthesis of coumarin derivatives. Coumarins are a class of compounds known for their diverse biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. By modifying the bromo and methoxy groups on the chromenone ring, chemists can access a wide range of coumarin analogs with tailored properties for specific applications.Additionally, 3-Bromo-7-methoxy-4H-chromen-4-one can be utilized in the synthesis of complex heterocyclic compounds. Its bromo and methoxy functionalities serve as handles for further elaboration, enabling chemists to construct intricate molecular structures with multiple points of diversification. These heterocyclic compounds have applications in medicinal chemistry, agrochemicals, and materials science.Furthermore, this compound can also be employed in the development of fluorescent probes and dyes. By incorporating specific fluorescent moieties onto the chromenone scaffold, researchers can generate compounds that exhibit unique photophysical properties, making them valuable tools for biological imaging and sensing applications.In conclusion, the versatility of 3-Bromo-7-methoxy-4H-chromen-4-one in chemical synthesis makes it a valuable asset in the toolbox of synthetic chemists, enabling the construction of diverse molecular architectures with potential implications in drug discovery, materials science, and other fields of research.