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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)-

Benzenepropanoic acid, 4-fluoro-, ethyl ester

CCOC(=O)CCc1ccc(cc1)F Request for Quotation
Chemical Name: Benzenepropanoic acid, 4-fluoro-, ethyl ester
CAS Number: 7116-38-3
Product Number: AG005X5K(AGN-PC-00GR69)
Synonyms:
MDL No:
Molecular Formula: C11H13FO2
Molecular Weight: 196.2181

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
196.221g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
196.09g/mol
Monoisotopic Mass:
196.09g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
174
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 3-(4-fluorophenyl)propanoate is a versatile compound used in chemical synthesis as a key intermediate for the production of various pharmaceuticals, agrochemicals, and fine chemicals. This compound plays a crucial role in organic synthesis due to its ability to undergo various chemical transformations, such as esterification, oxidation, reduction, and halogenation.In pharmaceutical synthesis, Ethyl 3-(4-fluorophenyl)propanoate serves as a building block for the creation of potential drug candidates, targeting a wide range of therapeutic areas including cardiovascular diseases, cancer, and neurological disorders. By incorporating this compound into the molecular structure of drug molecules, chemists can modulate the pharmacological properties of the final product, improving its efficacy and bioavailability.Furthermore, in agrochemical synthesis, Ethyl 3-(4-fluorophenyl)propanoate can be utilized to synthesize novel pesticides, herbicides, and fungicides with enhanced performance and environmental safety profiles. This compound enables chemists to design new active ingredients that effectively control pests and diseases in agricultural crops while minimizing adverse effects on non-target organisms and ecosystems.Overall, the application of Ethyl 3-(4-fluorophenyl)propanoate in chemical synthesis exemplifies its significance as a valuable building block for the creation of complex molecules with diverse functionalities and potential applications in the fields of pharmaceuticals, agrochemicals, and fine chemicals.