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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)-

2-bromo-5-iodo-3-methoxypyridine

COc1cc(I)cnc1Br Request for Quotation
Chemical Name: 2-bromo-5-iodo-3-methoxypyridine
CAS Number: 1131335-43-7
Product Number: AG003GPW(AGN-PC-07XSI8)
Synonyms:
MDL No:
Molecular Formula: C6H5BrINO
Molecular Weight: 313.9185

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
313.92g/mol
XLogP3:
2.5
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-5-iodo-3-methoxypyridine is a valuable compound widely used in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a key component in the generation of diverse chemical compounds with various applications.In the field of pharmaceuticals, 2-Bromo-5-iodo-3-methoxypyridine serves as a crucial intermediate in the synthesis of bioactive molecules and drug candidates. Its presence enables the introduction of specific functional groups or modifications essential for enhancing biological activity or improving pharmacokinetic properties.Furthermore, this compound plays a significant role in agrochemical synthesis, where it contributes to the development of novel pesticides, herbicides, and fungicides. By incorporating 2-Bromo-5-iodo-3-methoxypyridine into the molecular structure of these chemicals, researchers can tailor their properties to target specific pests or pathogens effectively.Additionally, in the realm of material science, 2-Bromo-5-iodo-3-methoxypyridine finds applications in the production of specialty chemicals, polymers, and advanced materials. Its ability to undergo various reactions and form intricate bonds allows for the creation of tailored materials with specific properties, such as conductivity, thermal stability, or optical characteristics.Overall, the versatility and reactivity of 2-Bromo-5-iodo-3-methoxypyridine make it a valuable tool in chemical synthesis across multiple industries, enabling the development of innovative compounds with diverse applications.