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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, 2,4,5-trifluoro-

Fc1ncc(c(n1)F)F Request for Quotation
Chemical Name: Pyrimidine, 2,4,5-trifluoro-
CAS Number: 17573-79-4
Product Number: AG00215H(AGN-PC-0NKBOC)
Synonyms:
MDL No:
Molecular Formula: C4HF3N2
Molecular Weight: 134.0593

Identification/Properties

Computed Properties
Molecular Weight:
134.061g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
134.009g/mol
Monoisotopic Mass:
134.009g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
99.8
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


2,4,5-Trifluoropyrimidine is a versatile compound widely used in chemical synthesis as a key building block for the production of various compounds. Its unique structure, containing three fluorine atoms and a pyrimidine ring, lends itself to a variety of reactions and transformations in organic chemistry.In chemical synthesis, 2,4,5-Trifluoropyrimidine serves as a valuable intermediate for the construction of complex molecules, particularly in the pharmaceutical and agrochemical industries. Its fluorinated nature imparts special properties to the final products, such as increased stability and altered reactivity compared to non-fluorinated analogs. This makes it a valuable tool for creating new drugs, crop protection agents, and other specialty chemicals.Additionally, 2,4,5-Trifluoropyrimidine can participate in diverse synthetic pathways, including nucleophilic substitution, palladium-catalyzed coupling reactions, and various functional group transformations. Its versatility and compatibility with a range of synthetic methods make it a highly sought-after compound for organic chemists seeking to access novel structures and functionalities in their target molecules.