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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-(4-fluorophenyl)pyridine-4-carbaldehyde

O=Cc1ccnc(c1)c1ccc(cc1)F Request for Quotation
Chemical Name: 2-(4-fluorophenyl)pyridine-4-carbaldehyde
CAS Number: 1214368-14-5
Product Number: AG0014WC(AGN-PC-07QWSK)
Synonyms:
MDL No:
Molecular Formula: C12H8FNO
Molecular Weight: 201.1964

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Fluorophenyl)isonicotinaldehyde is a versatile compound widely used in chemical synthesis for various applications. This aldehyde derivative plays a crucial role in the pharmaceutical industry, where it is frequently utilized as a key intermediate in the synthesis of numerous biologically active molecules. Its unique structure contains both a fluorophenyl group and an isonicotinaldehyde functionality, allowing for selective reactions and the formation of intricate chemical structures.In organic synthesis, 2-(4-Fluorophenyl)isonicotinaldehyde serves as a valuable building block for creating diverse compounds with specific properties. Its aldehyde group can undergo various types of reactions, including condensation, reduction, and oxidation, enabling the introduction of new functional groups or modifications to the existing structure. This compound is particularly valuable in medicinal chemistry for designing novel drugs or pharmaceutical compounds due to its ability to participate in key synthetic pathways and form essential pharmacophores.Furthermore, the presence of the fluorophenyl moiety in 2-(4-Fluorophenyl)isonicotinaldehyde confers additional properties that can be exploited in chemical synthesis. Fluorine is well-known for its unique effects on molecular reactivity, stability, and bioavailability, making compounds containing fluorine atoms highly valuable in drug discovery and development. By incorporating 2-(4-Fluorophenyl)isonicotinaldehyde into synthetic routes, chemists can harness the fluorine's beneficial characteristics to enhance the biological activity or physicochemical properties of the final products.Overall, 2-(4-Fluorophenyl)isonicotinaldehyde is a pivotal compound in chemical synthesis with diverse applications in pharmaceutical research, materials science, and agrochemical development. Its strategic positioning as an intermediate allows for efficient access to complex molecules, making it an indispensable tool for chemists seeking to create innovative compounds with tailored functionalities.