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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, 4-ethoxy-3-nitro-, monohydrochloride

CCOc1ccncc1[N+](=O)[O-].Cl Request for Quotation
Chemical Name: Pyridine, 4-ethoxy-3-nitro-, monohydrochloride
CAS Number: 94602-04-7
Product Number: AG003LB5(AGN-PC-0W48KU)
Synonyms:
MDL No:
Molecular Formula: C7H9ClN2O3
Molecular Weight: 204.6110

Identification/Properties

Properties
MP:
270-272 °C
BP:
319.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
204.61g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
204.03g/mol
Monoisotopic Mass:
204.03g/mol
Topological Polar Surface Area:
67.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
157
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Ethoxy-3-nitropyridine hydrochloride is a critical intermediate in organic synthesis, widely used in the pharmaceutical and agrochemical industries. This compound serves as a versatile building block for the preparation of various functionalized molecules due to its unique structural characteristics.Its primary application lies in the field of chemical synthesis, where it acts as a key component in the construction of complex organic compounds. Specifically, 4-Ethoxy-3-nitropyridine hydrochloride can participate in a range of reactions such as substitution, reduction, and coupling processes, enabling the formation of new carbon-carbon and carbon-heteroatom bonds.In pharmaceutical synthesis, this compound plays a crucial role in the development of biologically active molecules, including potential drug candidates. By incorporating 4-Ethoxy-3-nitropyridine hydrochloride into the molecular framework, medicinal chemists can modulate the physicochemical properties and biological activities of the resulting compounds, leading to the discovery of novel therapeutic agents.Furthermore, in agrochemical synthesis, this compound can be utilized to design pesticides, herbicides, and fungicides with improved efficacy and specificity. Its structural features allow for the introduction of functional groups that can enhance the bioactivity and environmental profile of the final products, contributing to sustainable agriculture practices.Overall, 4-Ethoxy-3-nitropyridine hydrochloride is a valuable tool in chemical synthesis, enabling the efficient and strategic construction of diverse organic molecules with applications spanning pharmaceuticals, agrochemicals, and materials science.