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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)-

4-Pyridinamine, 3,5-diiodo-

Ic1cncc(c1N)I Request for Quotation
Chemical Name: 4-Pyridinamine, 3,5-diiodo-
CAS Number: 98136-86-8
Product Number: AG003KP2(AGN-PC-05WHW3)
Synonyms:
MDL No: MFCD02663851
Molecular Formula: C5H4I2N2
Molecular Weight: 345.9076

Identification/Properties

Properties
MP:
135-136℃
BP:
408.1°C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
345.91g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
345.846g/mol
Monoisotopic Mass:
345.846g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
89
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


4-Amino-3,5-Diiodopyridine is a versatile chemical compound that finds extensive application in chemical synthesis processes. As a key building block in organic chemistry, it is utilized in the development of pharmaceuticals, agrochemicals, and materials science. This compound serves as a valuable intermediate in the synthesis of various compounds, owing to its unique structural properties and reactivity. In organic synthesis, 4-Amino-3,5-Diiodopyridine acts as a crucial reagent for the construction of complex molecular structures through a variety of reactions, including nucleophilic substitution, cross-coupling, and cyclization reactions. Its presence in the synthesis pathway enables the creation of novel compounds with diverse functionalities and applications in the fields of medicinal chemistry, drug discovery, and material design. By incorporating 4-Amino-3,5-Diiodopyridine into chemical reactions, researchers and chemists can access a wide range of molecular scaffolds that are essential for the development of new pharmaceuticals, crop protection agents, and advanced materials.