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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)-

5-bromo-3-iodo-6-methylpyridin-2-amine

Brc1cc(I)c(nc1C)N Request for Quotation
Chemical Name: 5-bromo-3-iodo-6-methylpyridin-2-amine
CAS Number: 958357-86-3
Product Number: AG006AS1(AGN-PC-04Q67W)
Synonyms:
MDL No:
Molecular Formula: C6H6BrIN2
Molecular Weight: 312.9337

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
312.936g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
311.876g/mol
Monoisotopic Mass:
311.876g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
122
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-3-iodo-6-methylpyridin-2-amine is a versatile compound that finds widespread applications in chemical synthesis. This compound is commonly utilized as a building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural properties.In chemical synthesis, 5-Bromo-3-iodo-6-methylpyridin-2-amine serves as a key starting material for the preparation of complex organic molecules. Its functional groups, the bromo and iodo substituents, enable selective modification through various chemical reactions such as cross-coupling reactions, halogenation, and substitution reactions. These reactions allow for the systematic manipulation of the compound's structure to introduce desired characteristics or functionalities.Furthermore, the presence of the pyridine ring in the molecule imparts specific chemical reactivity, making it a valuable intermediate for the synthesis of heterocyclic compounds, which are prevalent in pharmaceutical and agrochemical industries. The ability to derivatize this compound with different functional groups further enhances its utility in designing novel compounds with targeted biological activities.Overall, the strategic incorporation of 5-Bromo-3-iodo-6-methylpyridin-2-amine into synthetic pathways enables chemists to access a diverse array of structurally complex molecules with potential applications in drug discovery, material science, and other chemical sectors.