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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)-

3-fluoropyridine-2,6-diamine

Nc1ccc(c(n1)N)F Request for Quotation
Chemical Name: 3-fluoropyridine-2,6-diamine
CAS Number: 960138-28-7
Product Number: AG0069LR(AGN-PC-09S276)
Synonyms:
MDL No:
Molecular Formula: C5H6FN3
Molecular Weight: 127.1196

Identification/Properties

Properties
BP:
270.2±35.0°C at 760 mmHg
Computed Properties
Molecular Weight:
127.122g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
127.055g/mol
Monoisotopic Mass:
127.055g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
98.2
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


3-Fluoropyridine-2,6-diamine, also known as $name$, is a valuable building block in chemical synthesis due to its unique properties and reactivity. This compound serves as a versatile intermediate in the creation of various functional molecules, particularly in the field of medicinal chemistry and materials science.One key application of 3-Fluoropyridine-2,6-diamine is its use as a starting material for the synthesis of heterocyclic compounds. By incorporating this molecule into the reaction pathway, chemists can introduce fluorine atoms into the final product, imparting desirable properties such as improved stability and enhanced biological activity. Additionally, the presence of amino groups in this compound allows for further functionalization, enabling the introduction of diverse chemical functionalities for tailored applications.Furthermore, 3-Fluoropyridine-2,6-diamine plays a crucial role in the development of pharmaceutical agents and agrochemicals. Its fluorinated structure can enhance the pharmacokinetic properties of drug candidates, leading to increased efficacy and reduced side effects. By leveraging the versatility of this compound in chemical synthesis, researchers can access a wide range of novel compounds with potential applications in drug discovery and agricultural innovation.