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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-Pyridinecarboxaldehyde, 6-fluoro-

O=Cc1cccc(n1)F Request for Quotation
Chemical Name: 2-Pyridinecarboxaldehyde, 6-fluoro-
CAS Number: 208110-81-0
Product Number: AG002JHD(AGN-PC-0N7FDR)
Synonyms:
MDL No: MFCD03095149
Molecular Formula: C6H4FNO
Molecular Weight: 125.1005

Identification/Properties

Properties
BP:
192.4°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
125.102g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
125.028g/mol
Monoisotopic Mass:
125.028g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
107
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


6-Fluoropyridine-2-carboxaldehyde, also known as $name$, is a versatile chemical compound widely utilized in chemical synthesis processes. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique properties and reactivity.1. Heterocyclic Chemistry:
The presence of the pyridine ring in 6-Fluoropyridine-2-carboxaldehyde makes it an essential component in the synthesis of heterocyclic compounds. These compounds play a key role in drug discovery and development, as many bioactive molecules contain heterocyclic moieties.2. Fluorination Reactions:
The fluorine atom in the compound's structure imparts specific properties that are highly desirable in organic synthesis. Fluorinated compounds are often used in medicinal chemistry to enhance the bioavailability, metabolic stability, and binding affinity of drug candidates.3. Cross-Coupling Reactions:
6-Fluoropyridine-2-carboxaldehyde is frequently employed as a coupling partner in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. These reactions enable the formation of carbon-carbon and carbon-heteroatom bonds, facilitating the construction of complex organic molecules.4. Ligand Synthesis:
The aldehyde functional group in $name$ can serve as a versatile handle for further functionalization, leading to the synthesis of ligands for catalysis and coordination chemistry. Ligands derived from this compound are valuable tools in asymmetric synthesis and transition metal-catalyzed reactions.5. Agrochemical Development:
The ability to introduce fluorine atoms into agrochemical compounds enhances their biological activity and environmental properties. By incorporating 6-Fluoropyridine-2-carboxaldehyde into the synthesis of agrochemicals, researchers can develop more effective and sustainable crop protection products.Overall, the diverse applications of 6-Fluoropyridine-2-carboxaldehyde in chemical synthesis underscore its significance in modern organic chemistry and its pivotal role in advancing various scientific fields.