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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)-

Benzene, 1-(2-methoxyethoxy)-4-nitro-

COCCOc1ccc(cc1)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzene, 1-(2-methoxyethoxy)-4-nitro-
CAS Number: 22483-40-5
Product Number: AG007OER(AGN-PC-0JSP6H)
Synonyms:
MDL No:
Molecular Formula: C9H11NO4
Molecular Weight: 197.1879

Identification/Properties

Computed Properties
Molecular Weight:
197.19g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
197.069g/mol
Monoisotopic Mass:
197.069g/mol
Topological Polar Surface Area:
64.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
172
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


1-(2-Methoxyethoxy)-4-nitrobenzene, also known as phenyl 4-nitrophenyl ether, plays a crucial role in chemical synthesis as a versatile building block. Its unique chemical structure allows it to be utilized in a wide range of applications within the field of organic chemistry.This compound is commonly employed as a valuable intermediate in the synthesis of various organic compounds, particularly in the preparation of pharmaceuticals, agrochemicals, and advanced materials. Its nitro group provides a handle for various transformations such as reduction, substitution, or coupling reactions, enabling the creation of diverse molecular structures with specific properties.Furthermore, the methoxyethoxy side chain enhances the compound's solubility and stability in different solvents, making it a convenient choice for synthetic chemists. By incorporating 1-(2-Methoxyethoxy)-4-nitrobenzene into synthetic pathways, researchers can access novel molecules with tailored properties and functionalities, opening up new possibilities for drug discovery, material science, and other chemical applications.