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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)-

Benzofuran, 4-bromo-7-chloro-

Brc1ccc(c2c1cco2)Cl Request for Quotation
Chemical Name: Benzofuran, 4-bromo-7-chloro-
CAS Number: 855343-01-0
Product Number: AG00GN0T(AGN-PC-0BYEP7)
Synonyms:
MDL No:
Molecular Formula: C8H4BrClO
Molecular Weight: 231.4738

Identification/Properties

Computed Properties
Molecular Weight:
231.473g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
229.913g/mol
Monoisotopic Mass:
229.913g/mol
Topological Polar Surface Area:
13.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-7-chlorobenzofuran is a versatile compound widely used in chemical synthesis for various applications. This compound serves as a valuable building block in the creation of novel molecules and pharmaceuticals. Due to its unique structure, 4-Bromo-7-chlorobenzofuran can participate in diverse organic reactions, offering a range of possibilities for the formation of complex chemical structures. Its incorporation into synthesis routes allows for the generation of compounds with specific properties and functions, making it a vital component in the production of fine chemicals and drug intermediates. In addition, the presence of both bromine and chlorine atoms in 4-Bromo-7-chlorobenzofuran enhances its reactivity and enables the introduction of functional groups with precision, facilitating the synthesis of target molecules with high efficiency and selectivity. This compound plays a crucial role in the advancement of modern organic chemistry and drug discovery efforts, offering synthetic chemists a powerful tool for the design and construction of sophisticated molecules with potential therapeutic applications.