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  2. ethyl 4-(2,6-dichloro-5-fluoropyridin-3-yl)-3-oxobutanoate

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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)-

ethyl 4-(2,6-dichloro-5-fluoropyridin-3-yl)-3-oxobutanoate

CCCC(=O)OC(=O)c1cc(F)c(nc1Cl)Cl Request for Quotation
Chemical Name: ethyl 4-(2,6-dichloro-5-fluoropyridin-3-yl)-3-oxobutanoate
CAS Number: 96568-04-6
Product Number: AG003Q2N(AGN-PC-0NP8DT)
Synonyms:
MDL No:
Molecular Formula: C10H8Cl2FNO3
Molecular Weight: 280.0798

Identification/Properties

Properties
MP:
68-72 °C(lit.)
BP:
363.4±37.0°C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
280.076g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
278.987g/mol
Monoisotopic Mass:
278.987g/mol
Topological Polar Surface Area:
56.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
303
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-(2,6-Dichloro-5-fluoro-3-pyridyl)-3-oxopropionate is a valuable compound commonly used in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its versatile reactivity and functional group compatibility make it a crucial intermediate in the synthesis of biologically active compounds.This compound plays a crucial role in the synthesis of pyridine derivatives, which are important scaffolds found in many pharmaceutical agents and agricultural chemicals. By leveraging the unique reactivity of Ethyl 3-(2,6-Dichloro-5-fluoro-3-pyridyl)-3-oxopropionate, chemists can access a diverse array of functionalized pyridine derivatives through various synthetic strategies.Furthermore, Ethyl 3-(2,6-Dichloro-5-fluoro-3-pyridyl)-3-oxopropionate can be utilized in the construction of complex heterocyclic systems, which are prevalent in medicinal chemistry and materials science. Its incorporation into multistep synthetic routes allows for the efficient assembly of target molecules with desired pharmacological or physicochemical properties.In summary, the strategic incorporation of Ethyl 3-(2,6-Dichloro-5-fluoro-3-pyridyl)-3-oxopropionate in chemical synthesis enables the streamlined access to a wide range of valuable compounds with applications in drug discovery, crop protection, and materials research.