| Weight | 203.197 g/mol |
|---|---|
| Formula | C11H9NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
2-Methoxy-1-nitronaphthalene (4900-66-7)
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- Aromatic nucleophilic substitution. XIX: Kinetics of the formation and decomposition of 1,1-disubstituted naphthalene Meisenheimer complexes in the reactions of 1-methoxy-2-cyano-4-nitronaphthalene with various metal methoxides in methanol. Evidence for absence of ion pairing of Meisenheimer complexes with counterions (Journal of Organic Chemistry, 1981)
- Stereochemistry of protonation at C(1) of nitronate adducts from 1,6-conjugate addition of Grignard reagents to 2-methoxy-1-nitronaphthalene (Journal of The Chemical Society-perkin Transactions 1, 1984)
- Crystal structure of methyl 1,1,7,9-tetranitro-2,5-epoxy-1,2,4,5-tetrahydro-3,2-benzoxazepine-4-carboxylate, a product of nitration of 2-methoxy-1-nitronaphthalene (Journal of The Chemical Society, Chemical Communications, 1991)
- Kinetics and Mechanism of the Interaction of Methoxide Ions with 1-Methoxy-2-nitrobenzene and 1-Methoxy-2-nitronaphthalene in Methanol* (Zeitschrift fr Physikalische Chemie, 1969)
- ChemInform Abstract: STEREOCHEMISTRY OF PROTONATION AT C-1 OF NITRONATE ADDUCTS FROM 1,6-CONJUGATE ADDITION OF GRIGNARD REAGENTS TO 2-METHOXY-1-NITRONAPHTHALENE (ChemInform, 1984)
- ChemInform Abstract: Crystal Structure of Methyl 1,1,7,9-Tetranitro-2,5-epoxy-1,2,4,5- tetrahydro-3,2-benzoxazepine-4-carboxylate, a Product of Nitration of 2-Methoxy-1-nitronaphthalene. (ChemInform, 2010)
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SMILESCOC1=C(C2=CC=CC=C2C=C1)[N+](=O)[O-]
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InChIKeyXDNSKIDXVJNJFO-UHFFFAOYSA-N
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