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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-3-iodo-5-methyl-

Cc1cnc(c(c1)I)Br Request for Quotation
Chemical Name: Pyridine, 2-bromo-3-iodo-5-methyl-
CAS Number: 65550-82-5
Product Number: AG003GMX(AGN-PC-067UC4)
Synonyms:
MDL No:
Molecular Formula: C6H5BrIN
Molecular Weight: 297.9191

Identification/Properties

Properties
MP:
84-86 °C
BP:
306.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
297.921g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
296.865g/mol
Monoisotopic Mass:
296.865g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
99.1
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

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-iodo-5-methylpyridine is a versatile chemical reagent commonly employed in the field of chemical synthesis. This unique compound exhibits valuable properties that make it well-suited for a range of synthetic applications. In organic chemistry, 2-Bromo-3-iodo-5-methylpyridine serves as a valuable building block for the synthesis of complex molecules and pharmaceutical intermediates. Its specific structure allows for various functional group transformations and the introduction of both bromine and iodine atoms into target molecules, enabling synthetic chemists to access a diverse array of chemical structures. Furthermore, the presence of the pyridine ring in this compound offers a unique reactivity profile, making it particularly useful in the construction of heterocyclic compounds. Its ability to participate in various types of chemical reactions, such as palladium-catalyzed cross-coupling reactions and nucleophilic substitutions, further expands its utility in organic synthesis.Overall, the application of 2-Bromo-3-iodo-5-methylpyridine in chemical synthesis demonstrates its importance as a key reagent for the efficient and versatile construction of complex organic molecules with diverse pharmacological and industrial applications.