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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)-

2-Benzofurancarboxylic acid, 5-bromo-

Brc1ccc2c(c1)cc(o2)C(=O)O Request for Quotation
Chemical Name: 2-Benzofurancarboxylic acid, 5-bromo-
CAS Number: 10242-11-2
Product Number: AG0007FF(AGN-PC-0JVNPM)
Synonyms:
MDL No:
Molecular Formula: C9H5BrO3
Molecular Weight: 241.0382

Identification/Properties

Computed Properties
Molecular Weight:
241.04g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
239.942g/mol
Monoisotopic Mass:
239.942g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
219
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:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromobenzofuran-2-carboxylic acid is a versatile building block in chemical synthesis, particularly in the field of organic chemistry. This compound is often utilized in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals due to its unique reactivity and structural properties.One key application of 5-Bromobenzofuran-2-carboxylic acid is in the synthesis of biologically active molecules. By incorporating this compound into the chemical structure of a target molecule, chemists can introduce specific functional groups or modify the molecular scaffold to enhance the desired biological activity. This strategic use of 5-Bromobenzofuran-2-carboxylic acid allows for the development of new drug candidates with improved pharmacological profiles.Furthermore, 5-Bromobenzofuran-2-carboxylic acid serves as a valuable intermediate in the synthesis of heterocyclic compounds. Its benzofuran core provides a unique platform for further derivatization and diversification, enabling the generation of structurally diverse compounds for various applications. This compound can undergo a range of synthetic transformations, such as substitution, coupling, and cyclization reactions, leading to the creation of novel molecules with potential biological or material properties.Overall, the versatile nature of 5-Bromobenzofuran-2-carboxylic acid makes it a valuable tool in chemical synthesis, offering chemists a wide array of opportunities to explore new avenues in drug discovery, materials science, and other research fields.