Methanone, (2,5-difluorophenyl)phenyl-


Chemical Name: Methanone, (2,5-difluorophenyl)phenyl-
CAS Number: 85068-36-6
Product Number: AG003FYD(AGN-PC-0JSATX)
Synonyms:
MDL No: MFCD00009899
Molecular Formula: C13H8F2O
Molecular Weight: 218.1988

Identification/Properties


Properties
Storage:
2-8℃;Keep in dry area;
Form:
Liquid
Computed Properties
Molecular Weight:
218.203g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
218.054g/mol
Monoisotopic Mass:
218.054g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
248
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
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



(2,5-Difluorophenyl)phenylmethanone, commonly known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure, characterized by the presence of two fluorine atoms and a phenyl group, imparts specific chemical properties that make it valuable in various synthetic pathways. In organic chemistry, (2,5-Difluorophenyl)phenylmethanone serves as a key building block for the synthesis of pharmaceuticals, agrochemicals, and materials.One important application of (2,5-Difluorophenyl)phenylmethanone is in the preparation of novel organic molecules for drug discovery. The presence of fluorine atoms in the compound enhances its bioavailability and metabolic stability, making it an attractive candidate for drug design. By incorporating (2,5-Difluorophenyl)phenylmethanone into the molecular structure of potential drug candidates, researchers can modify the pharmacokinetic properties and improve the overall efficacy of the compounds.Furthermore, (2,5-Difluorophenyl)phenylmethanone is frequently utilized in the synthesis of complex organic compounds with specific electronic and steric requirements. Its fluorinated phenyl group can influence the reactivity and selectivity of chemical reactions, allowing chemists to access challenging chemical transformations and control the formation of desired product regioisomers or stereoisomers.In summary, (2,5-Difluorophenyl)phenylmethanone plays a crucial role in modern chemical synthesis, offering synthetic chemists a valuable tool for designing new molecules with tailored properties for pharmaceutical, agricultural, and materials science applications.