Benzenepropanoic acid, 2-fluoro-b-oxo-, ethyl ester


Chemical Name: Benzenepropanoic acid, 2-fluoro-b-oxo-, ethyl ester
CAS Number: 1479-24-9
Product Number: AG001F9M(AGN-PC-0Q13KP)
Synonyms:
MDL No:
Molecular Formula: C11H11FO3
Molecular Weight: 210.2016

Identification/Properties


Properties
BP:
270.1°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.516(lit.)
Computed Properties
Molecular Weight:
210.204g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
210.069g/mol
Monoisotopic Mass:
210.069g/mol
Topological Polar Surface Area:
43.4A^2
Heavy Atom Count:
15
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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



Ethyl 3-(2-fluorophenyl)-3-oxo-propionate is a valuable compound with significant applications in chemical synthesis. Known for its versatile reactivity and structural properties, this compound serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, Ethyl 3-(2-fluorophenyl)-3-oxo-propionate plays a crucial role as a precursor in the preparation of complex organic molecules. Its unique structure containing a fluoro-phenyl group and a keto functional group allows for diverse functionalization and manipulation, enabling chemists to introduce specific moieties and create intricate carbon-carbon and carbon-heteroatom bonds.Due to its synthetic utility and stability, Ethyl 3-(2-fluorophenyl)-3-oxo-propionate is commonly utilized in the synthesis of bioactive compounds such as pharmaceuticals and biologically relevant molecules. Its involvement in the construction of heterocyclic scaffolds and chiral centers makes it a valuable tool for medicinal chemistry research and drug development.Furthermore, this compound's role in the preparation of complex natural products and synthetic intermediates highlights its importance in advancing the field of organic synthesis. With its ability to undergo various transformations and reactions under controlled conditions, Ethyl 3-(2-fluorophenyl)-3-oxo-propionate serves as a versatile and indispensable component in modern chemical transformations and synthetic strategies.