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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)-

Methanone, (4-aminophenyl)(4-fluorophenyl)-

Nc1ccc(cc1)C(=O)c1ccc(cc1)F Request for Quotation
Chemical Name: Methanone, (4-aminophenyl)(4-fluorophenyl)-
CAS Number: 10055-40-0
Product Number: AG0002BE(AGN-PC-0JT6WM)
Synonyms:
MDL No:
Molecular Formula: C13H10FNO
Molecular Weight: 215.2230

Identification/Properties

Computed Properties
Molecular Weight:
215.227g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
215.075g/mol
Monoisotopic Mass:
215.075g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
240
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (4-Aminophenyl)(4-fluorophenyl)methanone compound is widely utilized in chemical synthesis as a key intermediate in various organic reactions. Due to its unique chemical structure, it serves as a valuable building block in the creation of complex organic molecules. Specifically, this compound is frequently employed in the pharmaceutical industry for the synthesis of novel drug candidates. Additionally, its versatile reactivity makes it a crucial component in the development of agrochemicals and specialty chemicals. Furthermore, (4-Aminophenyl)(4-fluorophenyl)methanone is instrumental in the preparation of advanced materials such as polymers and dyes, showcasing its significance across diverse areas of chemical research and production.