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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)-

2-fluoro-4-(3-methoxyphenyl)benzoic acid

COc1cccc(c1)c1ccc(c(c1)F)C(=O)O Request for Quotation
Chemical Name: 2-fluoro-4-(3-methoxyphenyl)benzoic acid
CAS Number: 1178418-69-3
Product Number: AG009422(AGN-PC-09PV0R)
Synonyms:
MDL No:
Molecular Formula: C14H11FO3
Molecular Weight: 246.2337

Identification/Properties

Computed Properties
Molecular Weight:
246.237g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
246.069g/mol
Monoisotopic Mass:
246.069g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
295
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Fluoro-3'-methoxy-[1,1'-biphenyl]-4-carboxylic acid, commonly referred to as $name$, is a versatile compound utilized in various chemical synthesis processes. One of its key applications lies in its role as a building block in the synthesis of pharmaceutical intermediates and fine chemicals. Due to its unique structure and functional groups, this compound serves as a valuable precursor in the creation of complex molecules with desirable properties.In chemical synthesis, $name$ can be employed in the construction of diverse organic compounds through strategic functional group transformations and bond formations. Its fluorine and methoxy substituents confer distinct reactivity patterns that enable precise control over the synthesis process. By incorporating this carboxylic acid derivative into synthetic routes, chemists can access novel structures and tailor-made molecules for targeted applications in medicinal chemistry, materials science, and agrochemicals development.