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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)-

3-bromo-2-phenylpyridine

Brc1cccnc1c1ccccc1 Request for Quotation
Chemical Name: 3-bromo-2-phenylpyridine
CAS Number: 91182-50-2
Product Number: AG003J0T(AGN-PC-0KKP2P)
Synonyms:
MDL No:
Molecular Formula: C11H8BrN
Molecular Weight: 234.0919

Identification/Properties

Properties
BP:
296.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
234.096g/mol
XLogP3:
3.2
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


3-Bromo-2-phenylpyridine is a versatile chemical compound commonly used in chemical synthesis for its unique properties. This compound serves as a valuable building block in various organic reactions, enabling the synthesis of complex molecules with specific structural features. One of the key applications of 3-Bromo-2-phenylpyridine is in the field of pharmaceutical chemistry, where it is utilized in the synthesis of biologically active compounds such as pharmaceutical drugs. Its structural characteristics make it a useful intermediate in the creation of novel drug candidates with potential therapeutic benefits.Additionally, this compound plays a crucial role in the development of new materials. Its ability to participate in diverse chemical transformations allows for the creation of custom-designed molecules for applications in materials science. By incorporating 3-Bromo-2-phenylpyridine into the synthesis of polymers, catalysts, and other materials, researchers can tailor the properties of the final products to meet specific requirements.Moreover, 3-Bromo-2-phenylpyridine finds applications in agrochemical synthesis, where it contributes to the production of crop protection agents and agricultural chemicals. Its versatility as a substrate in various chemical reactions makes it an essential component in the development of efficient and environmentally friendly agricultural products.Overall, the wide range of applications of 3-Bromo-2-phenylpyridine in chemical synthesis highlights its importance in driving innovation across different industries, from pharmaceuticals to materials science to agriculture.