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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)-

Ethanone, 1-(2,4-dichloro-5-fluorophenyl)-

CC(=O)c1cc(F)c(cc1Cl)Cl Request for Quotation
Chemical Name: Ethanone, 1-(2,4-dichloro-5-fluorophenyl)-
CAS Number: 704-10-9
Product Number: AG003FQ9(AGN-PC-0JVJ6Y)
Synonyms:
MDL No:
Molecular Formula: C8H5Cl2FO
Molecular Weight: 207.0291

Identification/Properties

Properties
MP:
33-36 °C
BP:
167°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
n20/D 1.546(lit.)
Computed Properties
Molecular Weight:
207.025g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
205.97g/mol
Monoisotopic Mass:
205.97g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
186
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(2,4-Dichloro-5-fluorophenyl)ethanone, known for its diverse applications in chemical synthesis, plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials. As a key intermediate, it serves as a building block in the synthesis of complex organic compounds with specific functional groups. Its unique structure offers opportunities for selective modifications, enabling the creation of novel molecules with tailored properties.In chemical synthesis, 1-(2,4-Dichloro-5-fluorophenyl)ethanone acts as a versatile reagent for the introduction of the 2,4-dichloro-5-fluorophenyl moiety into target molecules. Its ability to undergo diverse reactions, such as nucleophilic additions, condensations, and cyclizations, allows for the construction of intricate molecular frameworks. By incorporating this compound into synthetic pathways, chemists can access a wide range of structurally diverse compounds that exhibit desired biological or physicochemical properties.Additionally, the presence of both electron-withdrawing and electron-donating substituents on the phenyl ring of 1-(2,4-Dichloro-5-fluorophenyl)ethanone enhances its reactivity and compatibility with a variety of reaction conditions. This reactivity profile makes it a valuable tool for the straightforward and efficient assembly of complex molecular architectures in medicinal chemistry, material science, and other interdisciplinary fields.