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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-methoxy-2-methyl-3-nitro-

COc1cccc(c1C)N(=O)=O Request for Quotation
Chemical Name: Benzene, 1-methoxy-2-methyl-3-nitro-
CAS Number: 4837-88-1
Product Number: AG003HMN(AGN-PC-0JLRFY)
Synonyms:
MDL No:
Molecular Formula: C8H9NO3
Molecular Weight: 167.1620

Identification/Properties

Properties
MP:
54-56 °C(lit.)
BP:
260.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
167.164g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
167.058g/mol
Monoisotopic Mass:
167.058g/mol
Topological Polar Surface Area:
55A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
166
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methyl-3-nitroanisole, a chemical compound commonly used in chemical synthesis processes, is a versatile building block in organic chemistry. Its unique structure and properties make it valuable for various applications in the chemical industry. Due to its electron-rich nature, 2-Methyl-3-nitroanisole is often utilized as a precursor in the synthesis of pharmaceutical intermediates, agrochemicals, and other fine chemicals. Its functional groups enable it to participate in various reactions, including nitration, halogenation, and coupling reactions, allowing for the creation of more complex molecules. Additionally, the presence of a nitro group in the molecule offers opportunities for further derivatization and modifications to tailor the compound for specific desired properties. Overall, 2-Methyl-3-nitroanisole plays a crucial role in the development of new compounds and is an essential component in modern chemical synthesis strategies.