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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)-

Pyrimidine, 4,6-difluoro-

Fc1ncnc(c1)F Request for Quotation
Chemical Name: Pyrimidine, 4,6-difluoro-
CAS Number: 2802-62-2
Product Number: AG00C14O(AGN-PC-0JMPND)
Synonyms:
MDL No:
Molecular Formula: C4H2F2N2
Molecular Weight: 116.0689

Identification/Properties

Properties
BP:
124.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
116.071g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
116.019g/mol
Monoisotopic Mass:
116.019g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
70.4
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


4,6-Difluoropyrimidine is a versatile chemical compound that finds wide applications in chemical synthesis. Primarily, this compound serves as a valuable building block in the creation of various pharmaceuticals and agrochemicals. With its unique structure containing two fluorine atoms in strategic positions, 4,6-Difluoropyrimidine offers significant opportunities for medicinal chemistry and drug development.In chemical synthesis, 4,6-Difluoropyrimidine can be utilized as a key intermediate in the construction of complex molecular structures. Its presence can enhance the reactivity and selectivity of certain reactions, leading to the formation of novel compounds with desired properties. Furthermore, the introduction of fluorine atoms can impart specific functionalities to the final products, influencing their biological activity and stability.Overall, the incorporation of 4,6-Difluoropyrimidine in chemical synthesis processes enables researchers to access a diverse array of compounds with potential applications in the fields of medicine, agriculture, and materials science. Its role as a valuable building block underscores its importance in the development of innovative and high-impact chemical products.