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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-bromo-3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Brc1ncc(cc1F)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 2-bromo-3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
CAS Number: 1264130-85-9
Product Number: AG009BSX(AGN-PC-09SIGA)
Synonyms:
MDL No:
Molecular Formula: C11H14BBrFNO2
Molecular Weight: 301.9478

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-Bromo-3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile reagent in chemical synthesis, particularly in the field of organic chemistry. This compound is a key building block in the preparation of various biologically active molecules, pharmaceuticals, and agrochemicals. Its unique structure allows for selective functionalization, enabling the introduction of specific functional groups at precise positions within the molecule. This reagent is especially valuable in cross-coupling reactions, where it participates in Suzuki-Miyaura coupling reactions to form carbon-carbon bonds efficiently. Additionally, the presence of the dioxaborolane moiety enhances the stability and reactivity of the compound, making it a valuable tool for synthetic chemists working on complex molecular architectures.