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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)-

(2Z)-4-methoxy-2-(nitrosomethylidene)-6-pyridin-2-yl-1H-pyridine

O/N=C/c1cc(OC)cc(n1)c1ccccn1 Request for Quotation
Chemical Name: (2Z)-4-methoxy-2-(nitrosomethylidene)-6-pyridin-2-yl-1H-pyridine
CAS Number: 21802-37-9
Product Number: AG00BE5H(AGN-PC-0LQHKW)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
229.239g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
229.085g/mol
Monoisotopic Mass:
229.085g/mol
Topological Polar Surface Area:
67.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
260
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


(E)-4-Methoxy[2,2′-bipyridine]-6-carboxaldehyde oxime is a versatile compound widely utilized in chemical synthesis for its unique properties. This compound serves as a valuable building block in the development of various organic molecules due to its ability to participate in a range of reactions, including condensation, substitution, and complexation processes.In chemical synthesis, (E)-4-Methoxy[2,2′-bipyridine]-6-carboxaldehyde oxime plays a crucial role as a key intermediate in the production of heterocyclic compounds and coordination complexes. Its presence enables the formation of intricate molecular structures with specific functionalities, making it indispensable in the creation of pharmaceuticals, agrochemicals, and advanced materials.Furthermore, the selectivity and reactivity of (E)-4-Methoxy[2,2′-bipyridine]-6-carboxaldehyde oxime make it a valuable tool for chemists seeking to design and synthesize novel compounds with tailored properties. Whether employed as a ligand in metal-catalyzed reactions or as a precursor for functionalized derivatives, this compound opens up a myriad of possibilities for synthetic chemists striving to expand the frontiers of chemical discovery.