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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)-

Ethyl 7-bromobenzofuran-2-carboxylate

CCOC(=O)c1cc2c(o1)c(Br)ccc2 Request for Quotation
Chemical Name: Ethyl 7-bromobenzofuran-2-carboxylate
CAS Number: 1033201-65-8
Product Number: AG007XUA(AGN-PC-07XTVV)
Synonyms:
MDL No:
Molecular Formula: C11H9BrO3
Molecular Weight: 269.0914

Identification/Properties

Computed Properties
Molecular Weight:
269.094g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
267.974g/mol
Monoisotopic Mass:
267.974g/mol
Topological Polar Surface Area:
39.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
244
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

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Chemical Structure


Ethyl 7-bromobenzofuran-2-carboxylate is a versatile compound widely used in chemical synthesis for the derivatives it can produce. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique chemical structure and reactivity. In organic synthesis, this compound can undergo various transformations such as nucleophilic substitution, Suzuki-Miyaura coupling, and Heck coupling reactions to generate diverse molecular structures with specific functionalities. Its application in the synthesis of heterocyclic compounds further highlights its importance in drug discovery and material science. The strategic incorporation of Ethyl 7-bromobenzofuran-2-carboxylate into synthetic routes enables chemists to design and construct complex molecules efficiently and selectively, making it a valuable tool in modern organic chemistry research and development.