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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-methoxy-3-nitropyridine-2-carbonitrile

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Chemical Name: 6-methoxy-3-nitropyridine-2-carbonitrile
CAS Number: 950778-43-5
Product Number: AG01FR45(AGN-PC-0WOKZY)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
179.13g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
179.033091g/mol
Monoisotopic Mass:
179.033091g/mol
Topological Polar Surface Area:
91.7Ų
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
241
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Methoxy-3-nitro-pyridine-2-carbonitrile is a versatile compound that finds wide application in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structural properties, this compound serves as a valuable building block in the preparation of complex organic molecules through sequential chemical transformations.One of the prominent applications of 6-Methoxy-3-nitro-pyridine-2-carbonitrile is in the synthesis of novel heterocyclic compounds. By utilizing the cyano group as a versatile functional handle, chemists can introduce diverse chemical moieties to the molecule, enabling the creation of structurally diverse and biologically active compounds. This compound serves as a valuable precursor for the synthesis of heterocycles, such as pyridines, pyrimidines, and quinolines, which are crucial scaffolds in drug discovery and development.Moreover, 6-Methoxy-3-nitro-pyridine-2-carbonitrile plays a significant role in the development of new agrochemicals. By incorporating this compound into the design of agrochemical intermediates, chemists can modulate the activity and specificity of pesticides and herbicides, leading to improved crop protection and agricultural sustainability. The presence of both a methoxy and nitro group in the molecule provides a strategic advantage in tuning the physicochemical properties and biological activities of the final products.In summary, the strategic placement of the methoxy, nitro, and cyano functional groups in 6-Methoxy-3-nitro-pyridine-2-carbonitrile confers it with immense synthetic utility in the construction of diverse chemical structures of pharmaceutical and agrochemical interest. This compound serves as a valuable tool for chemists engaged in the synthesis of biologically active molecules and functional materials, facilitating innovation and advancement in the field of organic chemistry.