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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)-

2,5-Dibromophenylboronic acid

Brc1ccc(c(c1)B(O)O)Br Request for Quotation
Chemical Name: 2,5-Dibromophenylboronic acid
CAS Number: 1008106-93-1
Product Number: AG0002XT(AGN-PC-0WA5R5)
Synonyms:
MDL No:
Molecular Formula: C6H5BBr2O2
Molecular Weight: 279.7217

Identification/Properties

Computed Properties
Molecular Weight:
279.722g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
279.873g/mol
Monoisotopic Mass:
277.875g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
134
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


2,5-Dibromophenylboronic acid is a versatile and important compound used in chemical synthesis, particularly in the field of organic chemistry. This compound is valued for its ability to act as a key building block in the synthesis of various organic molecules through Suzuki-Miyaura cross-coupling reactions.By serving as a boronic acid derivative, 2,5-Dibromophenylboronic acid participates in coupling reactions with aryl halides or vinyl halides, enabling the formation of carbon-carbon bonds. This process is crucial in the creation of complex organic compounds, pharmaceuticals, agrochemicals, and materials with specific properties.Additionally, 2,5-Dibromophenylboronic acid can be utilized in the development of novel materials, such as liquid crystals, polymers, and organic electronic devices. Its unique structure and reactivity make it a valuable tool for chemists and researchers looking to design and synthesize new molecules and materials with tailored properties for various applications in industry and academia.