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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)-

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

Brc1cncc(c1)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: Pyridine, 3-bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS Number: 452972-13-3
Product Number: AG0039FA(AGN-PC-0NHOB0)
Synonyms:
MDL No:
Molecular Formula: C11H15BBrNO2
Molecular Weight: 283.9573

Identification/Properties

Computed Properties
Molecular Weight:
283.96g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
283.038g/mol
Monoisotopic Mass:
283.038g/mol
Topological Polar Surface Area:
31.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
257
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


3-Bromo-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridine serves as a versatile building block in chemical synthesis, making it an indispensable tool for organic chemists. This compound is widely utilized in the formation of carbon-carbon and carbon-heteroatom bonds through various coupling reactions such as Suzuki-Miyaura cross-coupling and Heck coupling. Its unique boron functionality allows for efficient and selective transformations, enhancing the efficiency of synthetic routes. Additionally, the pyridine moiety in the molecule provides a handle for further functionalization, enabling the construction of complex molecular scaffolds with precision and control. In the realm of medicinal chemistry, this compound's synthetic utility contributes to the development of novel pharmaceuticals and biologically active molecules.