2H-1-Benzopyran-3-carboxylic acid, 6,8-dibromo-2-oxo-


Chemical Name: 2H-1-Benzopyran-3-carboxylic acid, 6,8-dibromo-2-oxo-
CAS Number: 3855-87-6
Product Number: AG003N1E(AGN-PC-0JVI9H)
Synonyms:
MDL No:
Molecular Formula: C10H4Br2O4
Molecular Weight: 347.9444

Identification/Properties


Properties
MP:
221-224℃
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
347.946g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
347.846g/mol
Monoisotopic Mass:
345.848g/mol
Topological Polar Surface Area:
63.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
366
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



6,8-Dibromo-2-oxo-2H-chromene-3-carboxylic acid is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it an essential building block in the synthesis of complex organic molecules. Specifically, 6,8-Dibromo-2-oxo-2H-chromene-3-carboxylic acid is often employed in the formation of heterocyclic compounds, which are important structural motifs found in many bioactive compounds. Additionally, this compound serves as a valuable starting material for the synthesis of drug candidates and other biologically active molecules. Its utility in chemical synthesis extends to the creation of novel materials with applications in diverse fields such as medicine, agriculture, and materials science. By incorporating 6,8-Dibromo-2-oxo-2H-chromene-3-carboxylic acid into synthetic pathways, chemists can access a wide range of functionalized compounds with strategic importance in various industries.