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Brc1cnc(nc1)C
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CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
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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)-

Benzoic acid, 4-fluoroiodo-

Fc1ccc(c(c1)I)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 4-fluoroiodo-
CAS Number: 56096-89-0
Product Number: AG003LD4(AGN-PC-0NJ9FN)
Synonyms:
MDL No:
Molecular Formula: C7H4FIO2
Molecular Weight: 266.0083

Identification/Properties

Properties
MP:
144 - 146 °C
BP:
309.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Stability:
Light Sensitive
Computed Properties
Molecular Weight:
266.01g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
265.924g/mol
Monoisotopic Mass:
265.924g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
163
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P261-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Fluoro-2-iodobenzoic acid, also known as $name$, serves as a versatile building block in organic synthesis due to its unique chemical properties. This compound is commonly employed in the preparation of various pharmaceuticals, agrochemicals, and functional materials.One key application of 4-Fluoro-2-iodobenzoic acid is its role as a precursor in the synthesis of biologically active molecules. By undergoing various functional group transformations, such as coupling reactions or substitution reactions, this compound can be used to introduce the fluoro and iodo groups into target molecules, imparting desired pharmacological properties.Furthermore, 4-Fluoro-2-iodobenzoic acid is often utilized in medicinal chemistry research to modify the structure of drug candidates for improved selectivity, potency, or pharmacokinetic properties. Its presence in the molecular structure can enhance the biological activity of the final compound through optimization of key interactions with the biological target.In addition to its applications in pharmaceuticals, 4-Fluoro-2-iodobenzoic acid is also valuable in material science for the synthesis of functionalized polymers, advanced materials, and specialty chemicals. Its ability to act as a versatile intermediate allows for the creation of tailor-made molecules with specific properties, leading to a wide range of potential applications in various industries.Overall, 4-Fluoro-2-iodobenzoic acid plays a crucial role in chemical synthesis by enabling the construction of complex molecules with desired functionalities for applications in drug discovery, materials science, and other fields. Its versatility and reactivity make it an essential component in the toolbox of synthetic chemists seeking to create innovative and valuable compounds.