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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)-

2,6-Pyridinediamine, 3,5-difluoro-

Fc1cc(F)c(nc1N)N Request for Quotation
Chemical Name: 2,6-Pyridinediamine, 3,5-difluoro-
CAS Number: 247069-27-8
Product Number: AG002P3P(AGN-PC-0N02K5)
Synonyms:
MDL No:
Molecular Formula: C5H5F2N3
Molecular Weight: 145.1101

Identification/Properties

Properties
MP:
160 °C
BP:
233.3°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
145.113g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
145.045g/mol
Monoisotopic Mass:
145.045g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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


2,6-Diamino-3,5-difluoropyridine is a versatile chemical compound that finds wide application in chemical synthesis. Its unique molecular structure makes it a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, 2,6-Diamino-3,5-difluoropyridine serves as a key intermediate in the construction of complex organic molecules. It can participate in a variety of reactions, such as nucleophilic substitution, condensation, and amine coupling, to introduce the fluorine atoms and amino groups present in its structure into target molecules. Due to its functional groups and reactivity, 2,6-Diamino-3,5-difluoropyridine is particularly useful in the synthesis of fluorinated compounds, which are important in medicinal chemistry for enhancing drug potency, metabolic stability, and lipophilicity. Additionally, the amino groups in the molecule can undergo further derivatization to introduce additional functionalities or to tailor the compound's properties for specific applications.Overall, the strategic incorporation of 2,6-Diamino-3,5-difluoropyridine in chemical synthesis enables the efficient construction of diverse molecular scaffolds with fluorine and amino functionalities, making it a valuable tool for synthetic chemists in the development of new and innovative materials and compounds.