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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-2-iodo-3-methoxypyridine

COc1cc(Br)cnc1I Request for Quotation
Chemical Name: 5-bromo-2-iodo-3-methoxypyridine
CAS Number: 944805-60-1
Product Number: AG00II7N(AGN-PC-04G0FZ)
Synonyms:
MDL No:
Molecular Formula: C6H5BrINO
Molecular Weight: 313.9185

Identification/Properties

Computed Properties
Molecular Weight:
313.92g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
312.86g/mol
Monoisotopic Mass:
312.86g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
114
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P280-P304+P340+P312-P305+P351+P338-P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-2-iodo-3-methoxypyridine is a valuable chemical compound widely utilized in chemical synthesis processes. Its unique structure and properties make it a versatile building block for the creation of various complex organic molecules. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials due to its functional groups that allow for facile modification and derivatization. In organic synthesis, 5-Bromo-2-iodo-3-methoxypyridine is commonly employed in cross-coupling reactions, nucleophilic substitutions, and palladium-catalyzed transformations to introduce specific functional groups or motifs into target molecules. Its presence in a synthesis pathway can significantly impact the efficiency and selectivity of the overall process, making it a valuable tool for chemists involved in medicinal chemistry, material science, and agrochemical research.