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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)-

Benzenamine, 4-(3-fluorophenoxy)-

Nc1ccc(cc1)Oc1cccc(c1)F Request for Quotation
Chemical Name: Benzenamine, 4-(3-fluorophenoxy)-
CAS Number: 307308-62-9
Product Number: AG003130(AGN-PC-00PAF4)
Synonyms:
MDL No: MFCD02663349
Molecular Formula: C12H10FNO
Molecular Weight: 203.2123

Identification/Properties

Computed Properties
Molecular Weight:
203.216g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
203.075g/mol
Monoisotopic Mass:
203.075g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
192
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(3-Fluorophenoxy)aniline, a versatile compound used in chemical synthesis, serves as a key building block in various organic reactions. This compound is commonly employed in the design and preparation of pharmaceuticals, agrochemicals, and materials science applications due to its unique structural properties. In organic synthesis, 4-(3-Fluorophenoxy)aniline acts as a valuable intermediate for the creation of complex molecules with specific functionalities. Its ability to participate in nucleophilic aromatic substitution reactions and other synthetic transformations makes it a valuable tool in the hands of chemists aiming to develop novel chemical entities. Additionally, its fluorinated phenyl ring provides enhanced reactivity and selectivity in various transformations, making it a sought-after reagent in modern chemical research.