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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)-

Pyridine, 2,6-dimethoxy-3-nitro-

COc1nc(OC)ccc1[N+](=O)[O-] Request for Quotation
Chemical Name: Pyridine, 2,6-dimethoxy-3-nitro-
CAS Number: 18677-41-3
Product Number: AG00APH9(AGN-PC-0JVCK2)
Synonyms:
MDL No:
Molecular Formula: C7H8N2O4
Molecular Weight: 184.1494

Identification/Properties

Computed Properties
Molecular Weight:
184.151g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
184.048g/mol
Monoisotopic Mass:
184.048g/mol
Topological Polar Surface Area:
77.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
182
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#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,6-Dimethoxy-3-nitropyridine is a versatile chemical compound widely used in organic synthesis. Its application in chemical reactions primarily lies in its role as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. The nitro group on the pyridine ring enables it to participate in multiple synthetic pathways, leading to the formation of various complex molecular structures. Specifically, 2,6-Dimethoxy-3-nitropyridine serves as a key intermediate in the synthesis of biologically active compounds and potential drug candidates. Its ability to undergo diverse chemical transformations makes it a valuable tool for organic chemists seeking to develop novel molecules with specific properties and functions.