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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)-

Phenol, 2-methoxy-4-nitro-

COc1cc(ccc1O)[N+](=O)[O-] Request for Quotation
Chemical Name: Phenol, 2-methoxy-4-nitro-
CAS Number: 3251-56-7
Product Number: AG003HIZ(AGN-PC-0JLQ8E)
Synonyms:
MDL No:
Molecular Formula: C7H7NO4
Molecular Weight: 169.1348

Identification/Properties

Properties
MP:
99-104 °C
BP:
335.2°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.5500 (estimate)
Computed Properties
Molecular Weight:
169.136g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
169.038g/mol
Monoisotopic Mass:
169.038g/mol
Topological Polar Surface Area:
75.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
167
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methoxy-4-nitrophenol, also known as MNPN, is a versatile compound used in various chemical synthesis processes. This compound serves as a key intermediate in the production of pharmaceuticals, dyes, and agrochemicals. In organic synthesis, 2-Methoxy-4-nitrophenol is employed as a building block to create more complex molecules through various chemical reactions like nucleophilic substitutions, reductions, and coupling reactions. Its presence as a nitro-substituted phenol provides a unique reactivity profile that can be harnessed for the selective modification of other organic compounds. Additionally, the methoxy group in the molecule enables specific functional group interconversions, making it a valuable tool for designing and constructing multifunctional organic molecules with targeted properties.