dimethyl 2-(4-nitro-1-oxoisoindolin-2-yl)pentanedioate
$338.00
CAS No.: 827026-43-7
Catalog No.: 192725
Purity: 95%
MF: C15H16N2O7
MW: 336.3
Storage: 2-8 degree Celsius
SMILES: [N+](=O)([O-])C1=C2CN(C(C2=CC=C1)=O)C(C(=O)OC)CCC(=O)OC
Catalog No.: 192725
Purity: 95%
MF: C15H16N2O7
MW: 336.3
Storage: 2-8 degree Celsius
SMILES: [N+](=O)([O-])C1=C2CN(C(C2=CC=C1)=O)C(C(=O)OC)CCC(=O)OC
dimethyl 2-(4-nitro-1-oxoisoindolin-2-yl)pentanedioate; CAS No.: 827026-43-7; dimethyl 2-(4-nitro-1-oxoisoindolin-2-yl)pentanedioate. PROPERTIES: This nitro-substituted isoindolinone dicarboxylate ester has molecular formula C15H15N3O7. It typically appears as a pale yellow crystalline powder. The dimethyl 2-(4-nitro-1-oxoisoindolin-2-yl)pentanedioate demonstrates limited water solubility but good solubility in common organic solvents like methanol and ethyl acetate. Its melting point ranges between 140-145 C, and it has a molecular weight of approximately 357.29 g/mol. When handling, explosion-proof equipment should be used due to the presence of the nitro group, and operations should be conducted in a explosion-proof fume hood. Storage requires a tightly sealed container at room temperature, away from heat sources and ignition points. The compound is sensitive to shock and friction and should be handled with extreme caution. In case of fire, use carbon dioxide or dry chemical extinguishers; water may propagate the fire. APPLICATIONS: The dimethyl 2-(4-nitro-1-oxoisoindolin-2-yl)pentanedioate serves as a synthetic intermediate in the production of antibacterial agents targeting multidrug-resistant Gram-negative bacteria where the nitro group is reduced to a nitroso moiety in the bacterial environment, generating reactive species that disrupt microbial membranes (as reported in antimicrobial research literature). The ester groups allow for further functionalization through hydrolysis or transesterification reactions. Additionally, the compound functions as a building block in the synthesis of nonlinear optical materials with second harmonic generation efficiencies exceeding 1.5 times that of urea, as described in materials science publications. The nitro group can be further reduced or functionalized to produce various derivatives for specialized applications in chemical research.
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