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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2H-1-Benzopyran-3-carboxylicacid, 6-bromo-8-methoxy-

COc1cc(Br)cc2c1OCC(=C2)C(=O)O Request for Quotation
Chemical Name: 2H-1-Benzopyran-3-carboxylicacid, 6-bromo-8-methoxy-
CAS Number: 885271-13-6
Product Number: AG0089P8(AGN-PC-00UY6I)
Synonyms:
MDL No:
Molecular Formula: C11H9BrO4
Molecular Weight: 285.0908

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-8-methoxy-2H-chromene-3-carboxylic acid is a versatile compound commonly used in chemical synthesis processes. Its unique structure containing a bromine atom, a methoxy group, and a chromene ring makes it a valuable building block for the synthesis of complex organic molecules. In chemical synthesis, 6-Bromo-8-methoxy-2H-chromene-3-carboxylic acid can serve as a key intermediate for the preparation of various heterocyclic compounds and pharmaceutical agents. Its bromine atom allows for further functionalization, enabling chemists to introduce additional substituents or modify its structure to achieve desired properties. This compound can be utilized in the development of new drugs, agrochemicals, and materials due to its structural diversity and reactivity. Chemists often employ 6-Bromo-8-methoxy-2H-chromene-3-carboxylic acid in multi-step synthesis routes to access intricate molecular frameworks for a wide range of applications in the field of organic chemistry.