1. Home
  2. 5-bromo-6-fluoropyridine-3-carbaldehyde

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

5-bromo-6-fluoropyridine-3-carbaldehyde

O=Cc1cnc(c(c1)Br)F Request for Quotation
Chemical Name: 5-bromo-6-fluoropyridine-3-carbaldehyde
CAS Number: 1211541-15-9
Product Number: AG00HFYT(AGN-PC-03EI71)
Synonyms:
MDL No:
Molecular Formula: C6H3BrFNO
Molecular Weight: 203.9965232

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The 5-Bromo-6-fluoronicotinaldehyde is a versatile chemical intermediate that finds wide application in organic synthesis. Its unique molecular structure, comprising a bromine and fluorine atom on a nicotinaldehyde scaffold, imparts both reactivity and selectivity in various chemical reactions.In chemical synthesis, 5-Bromo-6-fluoronicotinaldehyde serves as a valuable building block for the construction of complex molecules. Its bromine and fluorine functionalities can be strategically manipulated to introduce desired chemical transformations, such as halogenation reactions or cross-coupling processes. Furthermore, the presence of the aldehyde group allows for efficient functional group interconversion through a variety of chemical reactions, enabling the synthesis of diverse chemical entities.One notable application of 5-Bromo-6-fluoronicotinaldehyde is its utility in the synthesis of pharmaceutical intermediates. By judiciously incorporating this compound into a synthetic route, chemists can access key structural motifs necessary for the preparation of biologically active compounds. Additionally, its compatibility with a range of reaction conditions makes it a valuable tool for the construction of heterocyclic frameworks and scaffolds prevalent in medicinal chemistry.Overall, the strategic incorporation of 5-Bromo-6-fluoronicotinaldehyde in chemical synthesis enables the efficient and versatile construction of complex molecules with diverse functionalities, highlighting its significance in modern organic chemistry methodologies.