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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-6-[4-(trifluoromethyl)phenyl]-

FC(c1ccc(cc1)c1ncnc(c1)Cl)(F)F Request for Quotation
Chemical Name: Pyrimidine, 4-chloro-6-[4-(trifluoromethyl)phenyl]-
CAS Number: 659729-09-6
Product Number: AG00FEJF(AGN-PC-015B8A)
Synonyms:
MDL No:
Molecular Formula: C11H6ClF3N2
Molecular Weight: 258.6269

Identification/Properties

Computed Properties
Molecular Weight:
258.628g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
258.017g/mol
Monoisotopic Mass:
258.017g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
252
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-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-6-(4-(trifluoromethyl)phenyl)pyrimidine is a versatile compound used in various chemical syntheses. Its unique structure provides a valuable building block for the creation of new molecules in the field of organic chemistry. This compound is commonly employed in the pharmaceutical industry for the development of potential drug candidates due to its ability to serve as a key intermediate in the synthesis of biologically active compounds. Additionally, 4-Chloro-6-(4-(trifluoromethyl)phenyl)pyrimidine finds application in agrochemical research where it is utilized in the design and production of novel pesticides and herbicides. Its reactivity and compatibility with a wide range of functional groups make it a valuable tool for synthetic chemists seeking to create diverse molecular structures for various applications.