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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-chloro-2,6-diphenyl-

Clc1cc(nc(n1)c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: Pyrimidine, 4-chloro-2,6-diphenyl-
CAS Number: 29509-91-9
Product Number: AG002YLQ(AGN-PC-00H4IA)
Synonyms:
MDL No:
Molecular Formula: C16H11ClN2
Molecular Weight: 266.7249

Identification/Properties

Computed Properties
Molecular Weight:
266.728g/mol
XLogP3:
4.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
266.061g/mol
Monoisotopic Mass:
266.061g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
272
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-Chloro-2,6-diphenylpyrimidine is a versatile compound commonly utilized in chemical synthesis processes. Its significance lies in its ability to serve as a key intermediate in the production of various organic compounds. In particular, this compound is frequently employed in the pharmaceutical industry for the synthesis of biologically active molecules. Its unique chemical structure enables it to participate in a range of reactions, allowing for the creation of diverse molecular structures with specific desired properties. Additionally, 4-Chloro-2,6-diphenylpyrimidine is utilized in academic research settings for the development of novel synthetic methodologies and the discovery of new chemical entities. Its role in chemical synthesis highlights its importance as a valuable building block in the creation of a wide array of functional molecules.