CAS 4900-63-4
:1-Methoxy-4-nitronaphthalene
Description:
1-Methoxy-4-nitronaphthalene, with the CAS number 4900-63-4, is an organic compound characterized by its naphthalene backbone substituted with a methoxy group and a nitro group. This compound typically appears as a yellow to orange crystalline solid and is known for its aromatic properties. The methoxy group (-OCH3) enhances its solubility in organic solvents, while the nitro group (-NO2) contributes to its reactivity, particularly in electrophilic substitution reactions. The presence of both substituents can influence the compound's electronic properties, making it a useful intermediate in organic synthesis, particularly in the production of dyes, pharmaceuticals, and agrochemicals. Additionally, 1-Methoxy-4-nitronaphthalene may exhibit specific physical properties such as melting and boiling points, which are essential for its handling and application in laboratory settings. Safety considerations should be taken into account, as nitro compounds can be hazardous and may require proper storage and handling protocols.
Formula:C11H9NO3
InChI:InChI=1S/C11H9NO3/c1-15-11-7-6-10(12(13)14)8-4-2-3-5-9(8)11/h2-7H,1H3
InChI key:InChIKey=YFJKGPRYPHFGQD-UHFFFAOYSA-N
SMILES:COc1ccc(c2ccccc12)N(=O)=O
Synonyms:- 1-Nitro-4-methoxynaphthalene
- 4-Methoxy-1-nitronaphthalene
- Methyl 4-Nitronaphthyl Ether
- Methyl 4-nitro-1-naphthyl ether
- NSC 65626
- Naphthalene, 1-methoxy-4-nitro-
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Found 4 products.
1-Methoxy-4-nitronaphthalene
CAS:Formula:C11H9NO3Purity:96%Color and Shape:SolidMolecular weight:203.19411-Methoxy-4-nitronaphthalene
CAS:Formula:C11H9NO3Purity:96%Color and Shape:SolidMolecular weight:203.1971-Methoxy-4-nitronaphthalene
CAS:<p>1-Methoxy-4-nitronaphthalene is a yellow crystalline solid that belongs to the group of naphthalenes. It reacts with deionized water to give nitronaphthalene, which can be detected by ultrafast spectroscopy at constant temperature or by second-order rate constants. The nitro group can be reduced to an amine on treatment with phosphite or diphosphorylated. Nitro groups are also susceptible to nucleophilic attack by acetonitrile and ammonium nitrate, and can be photoreduced to the corresponding amino compound.</p>Formula:CH3OC10H6NO2Purity:Min. 95%Molecular weight:203.19 g/mol



