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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)-

4-chloro-2-methoxy-3-nitropyridine

COc1nccc(c1[N+](=O)[O-])Cl Request for Quotation
Chemical Name: 4-chloro-2-methoxy-3-nitropyridine
CAS Number: 934180-48-0
Product Number: AG003L3I(AGN-PC-0BUCUV)
Synonyms:
MDL No: MFCD17014990
Molecular Formula: C6H5ClN2O3
Molecular Weight: 188.5685

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
188.567g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
187.999g/mol
Monoisotopic Mass:
187.999g/mol
Topological Polar Surface Area:
67.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
173
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


4-Chloro-2-methoxy-3-nitropyridine, also known as $name$, is a versatile compound widely utilized in chemical synthesis applications. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure enables it to participate in a range of key reactions, making it an indispensable tool for organic chemists. Specifically, 4-Chloro-2-methoxy-3-nitropyridine can be employed in the synthesis of complex molecules through processes such as nucleophilic substitution, palladium-catalyzed coupling reactions, and heterocyclic transformations. Due to its functional groups and reactivity, this compound plays a crucial role in the development of novel compounds with potential therapeutic benefits and agricultural applications. In the realm of chemical synthesis, 4-Chloro-2-methoxy-3-nitropyridine is prized for its ability to facilitate the construction of intricate molecular structures, making it a valuable asset in the creation of new, innovative chemical compounds.