CAS 13772-63-9
:methyl 3-nitronaphthalene-1-carboxylate
Description:
Methyl 3-nitronaphthalene-1-carboxylate is an organic compound characterized by its structure, which includes a naphthalene ring substituted with a nitro group and a carboxylate ester functional group. This compound typically appears as a yellow to orange crystalline solid and is known for its aromatic properties. The presence of the nitro group introduces electron-withdrawing characteristics, influencing the compound's reactivity and polarity. Methyl 3-nitronaphthalene-1-carboxylate is often utilized in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Its solubility is generally moderate in organic solvents, while its stability can be affected by light and heat. Safety considerations should be taken into account, as nitro compounds can be hazardous, and appropriate handling procedures should be followed. Overall, this compound exemplifies the complexity and utility of substituted aromatic compounds in chemical research and industrial applications.
Formula:C12H9NO4
InChI:InChI=1/C12H9NO4/c1-17-12(14)11-7-9(13(15)16)6-8-4-2-3-5-10(8)11/h2-7H,1H3
SMILES:COC(=O)c1cc(cc2ccccc12)N(=O)=O
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Found 3 products.
1-Naphthalenecarboxylic acid, 3-nitro-, methyl ester
CAS:Formula:C12H9NO4Purity:95%Color and Shape:SolidMolecular weight:231.2042Methyl 3-nitro-1-naphthoate
CAS:Formula:C12H9NO4Purity:≥95%Color and Shape:Liquid, No data available.Molecular weight:231.207


