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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-(3,4-dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Brc1ccc(cc1Br)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 2-(3,4-dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number: 1075719-78-6
Product Number: AG0084LH(AGN-PC-07XUCC)
Synonyms:
MDL No:
Molecular Formula: C12H15BBr2O2
Molecular Weight: 361.8653

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(3,4-Dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a valuable building block in chemical synthesis, particularly in the field of organic chemistry. This compound is commonly utilized as a versatile reagent for Suzuki-Miyaura cross-coupling reactions, a pivotal synthetic method for forming carbon-carbon bonds. By acting as a boron source in these cross-coupling reactions, 2-(3,4-Dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane enables the selective and efficient creation of complex organic molecules with high precision. Its unique structure and reactivity make it an indispensable tool for the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties. Additionally, this compound's stability and ease of handling further enhance its usefulness in various chemical transformations, making it a favored choice for synthetic chemists seeking to access diverse chemical architectures with strategic control.