4-(6-chloropyridazin-3-yl)benzaldehyde


Chemical Name: 4-(6-chloropyridazin-3-yl)benzaldehyde
CAS Number: 914349-19-2
Product Number: AG00H12F(AGN-PC-07A1FE)
Synonyms:
MDL No:
Molecular Formula: C11H7ClN2O
Molecular Weight: 218.6391

Identification/Properties


Computed Properties
Molecular Weight:
218.64g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
218.025g/mol
Monoisotopic Mass:
218.025g/mol
Topological Polar Surface Area:
42.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
217
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:
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


Request for Quotation


Customer Feedback


Chemical Structure



4-(6-Chloropyridazin-3-yl)benzaldehyde is a crucial reagent in chemical synthesis, often utilized as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. This compound serves as a versatile intermediate with numerous applications in organic chemistry, particularly in the synthesis of heterocyclic compounds.In organic synthesis, 4-(6-Chloropyridazin-3-yl)benzaldehyde can undergo various reactions such as nucleophilic addition, condensation, and oxidation, allowing for the formation of diverse chemical structures. Its unique molecular structure makes it a valuable starting material for the preparation of biologically active molecules, including pharmaceuticals targeting specific biological pathways.The presence of both the pyridazinyl and aldehyde functional groups in this compound offers a wide range of synthetic possibilities, enabling chemists to introduce additional substituents and modify the chemical properties of the resulting products. By incorporating 4-(6-Chloropyridazin-3-yl)benzaldehyde into synthetic routes, researchers can access a myriad of derivatives with potential applications in drug discovery, material science, and other areas of chemical research.Overall, the strategic utilization of 4-(6-Chloropyridazin-3-yl)benzaldehyde in chemical synthesis facilitates the construction of complex molecular architectures and provides a platform for the development of novel compounds with diverse functionalities.