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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)-

6-Chloro-4-fluoronicotinaldehyde

Fc1cc(Cl)ncc1C=O Request for Quotation
Chemical Name: 6-Chloro-4-fluoronicotinaldehyde
CAS Number: 1060809-20-2
Product Number: AG00HARD(AGN-PC-0WAGWT)
Synonyms:
MDL No:
Molecular Formula: C6H3ClFNO
Molecular Weight: 159.5455232

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloro-4-fluoronicotinaldehyde is a versatile building block in chemical synthesis due to its unique properties and reactivity. Its ability to undergo various reactions makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and heterocyclic compounds.One of the key applications of 6-Chloro-4-fluoronicotinaldehyde is its use in the preparation of pyridine derivatives, which are essential structural motifs in medicinal chemistry. This compound can participate in the construction of complex molecules through transformations such as nucleophilic substitution, condensation reactions, and cyclizations. By manipulating the functional groups present on the aldehyde, chemists can access a diverse range of substituted pyridine derivatives with tailored properties.Furthermore, 6-Chloro-4-fluoronicotinaldehyde serves as a key starting material in the synthesis of bioactive compounds with potential pharmacological activities. Its fluorine and chlorine substituents can play a crucial role in modulating the biological properties of the final molecules, enhancing their efficacy and selectivity. By introducing specific functional groups at various positions of the pyridine ring, researchers can fine-tune the biological activity of the synthesized compounds for specific targets.Overall, the versatile nature of 6-Chloro-4-fluoronicotinaldehyde in chemical synthesis makes it an indispensable tool for the efficient construction of complex molecules with diverse applications in pharmaceutical and agrochemical industries.