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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,5-bromo-4,6-difluoro-

Fc1ncnc(c1Br)F Request for Quotation
Chemical Name: Pyrimidine,5-bromo-4,6-difluoro-
CAS Number: 946681-88-5
Product Number: AG003MIX(AGN-PC-0W4B0T)
Synonyms:
MDL No:
Molecular Formula: C4HBrF2N2
Molecular Weight: 194.9649

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
194.967g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
193.929g/mol
Monoisotopic Mass:
193.929g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
92.6
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


5-Bromo-4,6-difluoropyrimidine is a versatile chemical compound that finds wide application in chemical synthesis due to its unique reactivity and properties. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, 5-Bromo-4,6-difluoropyrimidine acts as a key intermediate for the synthesis of bioactive compounds such as antiviral drugs, anticancer agents, and antibiotics. Its halogen atoms provide opportunities for further functionalization, enabling the introduction of diverse functional groups to fine-tune the properties of the final products.Additionally, 5-Bromo-4,6-difluoropyrimidine can participate in cross-coupling reactions, nucleophilic substitutions, and other transformations to form complex molecular structures efficiently. Its fluorine atoms contribute to the compound's stability and lipophilicity, making it highly desirable for drug design and discovery applications.Overall, the use of 5-Bromo-4,6-difluoropyrimidine in chemical synthesis enables chemists to access a broad range of chemical space and expedite the development of novel compounds with potential therapeutic or industrial significance.