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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)-

Phosphonic acid, [(2-fluorophenyl)methyl]-, diethyl ester

CCOP(=O)(Cc1ccccc1F)OCC Request for Quotation
Chemical Name: Phosphonic acid, [(2-fluorophenyl)methyl]-, diethyl ester
CAS Number: 63909-54-6
Product Number: AG00IBAR(AGN-PC-004DBT)
Synonyms:
MDL No: MFCD22574982
Molecular Formula: C11H16FO3P
Molecular Weight: 246.2151

Identification/Properties

Computed Properties
Molecular Weight:
246.218g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
246.082g/mol
Monoisotopic Mass:
246.082g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
237
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Diethyl 2-Fluorobenzylphosphonate is a versatile compound widely used in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials. It serves as a valuable intermediate in organic reactions due to its unique structure and reactivity profile. This compound is particularly prized for its role in the synthesis of complex molecules with fluorine substituents, offering researchers a powerful tool for the design and development of novel compounds with desired properties. Its incorporation into organic synthesis routes allows for the introduction of the fluorobenzylphosphonate moiety, enabling the modification of molecular structures to enhance biological activity or material properties. By leveraging the functional groups present in Diethyl 2-Fluorobenzylphosphonate, chemists can efficiently access diverse chemical space and drive innovation in the fields of medicinal chemistry, materials science, and beyond.