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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, 2-bromo-6-phenyl-

Brc1cccc(n1)c1ccccc1 Request for Quotation
Chemical Name: Pyridine, 2-bromo-6-phenyl-
CAS Number: 39774-26-0
Product Number: AG0038RK(AGN-PC-07H9SO)
Synonyms:
MDL No:
Molecular Formula: C11H8BrN
Molecular Weight: 234.0919

Identification/Properties

Computed Properties
Molecular Weight:
234.096g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
232.984g/mol
Monoisotopic Mass:
232.984g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
154
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-Bromo-6-phenylpyridine is a versatile compound commonly utilized in chemical synthesis. Its primary application lies in its role as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. This compound's unique structure and reactivity make it an essential intermediate in the synthesis of complex molecules with diverse functionalities. Through strategic functionalization and manipulation of its chemical properties, 2-Bromo-6-phenylpyridine can be transformed into a wide range of valuable derivatives, facilitating the development of novel compounds with targeted properties and applications in medicinal chemistry, crop protection, and materials science. Its ability to participate in a variety of coupling reactions and transformations makes it a valuable tool for organic chemists seeking to access structurally intricate and biologically active compounds for research and development purposes.