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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)-

6-bromo-4-iodopyridine-3-carbonitrile

Brc1cc(I)c(cn1)C#N Request for Quotation
Chemical Name: 6-bromo-4-iodopyridine-3-carbonitrile
CAS Number: 1061357-87-6
Product Number: AG00HAS3(AGN-PC-09R4JA)
Synonyms:
MDL No:
Molecular Formula: C6H2BrIN2
Molecular Weight: 308.9020

Identification/Properties

Computed Properties
Molecular Weight:
308.904g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
307.845g/mol
Monoisotopic Mass:
307.845g/mol
Topological Polar Surface Area:
36.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
164
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-4-iodonicotinonitrile is a versatile chemical compound that finds wide application in the field of chemical synthesis. This compound serves as a valuable building block in the preparation of various organic molecules due to its unique structural properties.In chemical synthesis, 6-Bromo-4-iodonicotinonitrile can be utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its halogenated nitrile functionality allows for selective reactions that enable the introduction of desired functional groups with high efficiency and control.Furthermore, the presence of both bromine and iodine atoms in the molecule provides opportunities for further derivatization through diverse chemical transformations such as cross-coupling reactions, metal-catalyzed reactions, and nucleophilic substitutions. This facilitates the creation of structurally complex molecules for various applications in material science and drug discovery.Overall, the strategic incorporation of 6-Bromo-4-iodonicotinonitrile in chemical synthesis processes offers synthetic chemists a reliable and versatile tool to access a wide range of functionalized compounds with potential applications in the development of new materials and biologically active molecules.