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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-5-IODOPYRIDIN-3-AMINE

Nc1cnc(c(c1)I)Br Request for Quotation
Chemical Name: 6-BROMO-5-IODOPYRIDIN-3-AMINE
CAS Number: 697300-68-8
Product Number: AG00FE72(AGN-PC-09RP3C)
Synonyms:
MDL No:
Molecular Formula: C5H4BrIN2
Molecular Weight: 298.9071

Identification/Properties

Computed Properties
Molecular Weight:
298.909g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
297.86g/mol
Monoisotopic Mass:
297.86g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
101
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


6-Bromo-5-iodopyridin-3-amine is a versatile chemical compound commonly used in chemical synthesis for a variety of applications. Due to its unique molecular structure, this compound serves as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. In organic chemistry, 6-Bromo-5-iodopyridin-3-amine is particularly useful for introducing specific functional groups or substituents into a target molecule. Its presence enables the creation of complex molecular structures through various chemical transformations such as cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed reactions. Furthermore, the presence of both bromine and iodine atoms in 6-Bromo-5-iodopyridin-3-amine allows for diverse reactivity patterns, making it a valuable reagent in the synthesis of heterocyclic compounds and medicinal intermediates. Chemists can leverage its reactivity to selectively modify molecules and create novel compounds with enhanced properties or activities.Overall, the strategic utilization of 6-Bromo-5-iodopyridin-3-amine in chemical synthesis allows chemists to efficiently access a wide range of structurally diverse compounds, making it an indispensable tool in the pharmaceutical and agrochemical industries.