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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)-

Benzaldehyde, 4-(2-pyridinyloxy)-

O=Cc1ccc(cc1)Oc1ccccn1 Request for Quotation
Chemical Name: Benzaldehyde, 4-(2-pyridinyloxy)-
CAS Number: 194017-69-1
Product Number: AG00AP73(AGN-PC-0KZLUB)
Synonyms:
MDL No:
Molecular Formula: C12H9NO2
Molecular Weight: 199.2054

Identification/Properties

Properties
MP:
45 °C
BP:
344.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
199.209g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
199.063g/mol
Monoisotopic Mass:
199.063g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
200
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

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Chemical Structure


4-(Pyridin-2-yloxy)benzaldehyde is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This aldehyde derivative serves as a valuable building block in organic chemistry, particularly in the design and preparation of various functional molecules. In the realm of drug discovery and medicinal chemistry, 4-(Pyridin-2-yloxy)benzaldehyde is commonly employed as a key intermediate for the synthesis of pharmaceutical agents and bioactive compounds. Its aromatic structure and aldehyde group enable it to participate in diverse synthetic transformations, such as condensation reactions, oxidative processes, and metal-catalyzed coupling reactions. Additionally, the presence of the pyridine moiety offers specific coordination sites for metal catalysts, further expanding the range of potential applications in transition metal-catalyzed reactions. Researchers and chemists utilize 4-(Pyridin-2-yloxy)benzaldehyde as a crucial component in the development of novel organic molecules with desirable biological activities or functional properties.