CAS 53055-05-3
:3-Methoxy-2-nitrobenzaldehyde
Description:
3-Methoxy-2-nitrobenzaldehyde, with the CAS number 53055-05-3, is an organic compound characterized by its aromatic structure featuring both a methoxy group (-OCH₃) and a nitro group (-NO₂) attached to a benzaldehyde moiety. This compound typically appears as a yellow to orange crystalline solid and is known for its distinct aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic structure. The presence of the nitro group contributes to its electrophilic reactivity, making it useful in various chemical synthesis applications, including the preparation of dyes and pharmaceuticals. Additionally, the methoxy group can influence the compound's electronic properties and reactivity, often acting as a directing group in electrophilic aromatic substitution reactions. Safety precautions should be taken when handling this compound, as nitro compounds can be hazardous and may pose environmental risks.
Formula:C8H7NO4
InChI:InChI=1S/C8H7NO4/c1-13-7-4-2-3-6(5-10)8(7)9(11)12/h2-5H,1H3
InChI key:InChIKey=GDTUACILWWLIJF-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(C=O)C=CC=C1OC
Synonyms:- 2-Nitro-3-methoxybenzaldehyde
- Benzaldehyde, 3-methoxy-2-nitro-
- NSC 172558
- m-Anisaldehyde, 2-nitro-
- 3-Methoxy-2-nitrobenzaldehyde
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Found 4 products.
3-Methoxy-2-nitrobenzaldehyde
CAS:Formula:C8H7NO4Purity:97%Color and Shape:SolidMolecular weight:181.14553-Methoxy-2-nitrobenzaldehyde
CAS:<p>3-Methoxy-2-nitrobenzaldehyde</p>Formula:C8H7NO4Purity:98%Color and Shape: brown solidMolecular weight:181.15g/mol3-Methoxy-2-nitrobenzaldehyde
CAS:<p>3-Methoxy-2-nitrobenzaldehyde is a synthetic compound that has been used in the industrial process of synthesizing other compounds. It is a nucleophilic compound, which means it can react with electrophiles to form new bonds. 3-Methoxy-2-nitrobenzaldehyde is also an oriented molecule, meaning that when it reacts with an electrophile, the resulting product can be determined by the orientation of the molecules. The rate of this reaction depends on how many functional groups are present and the presence of catalysts. 3-Methoxy-2-nitrobenzaldehyde is fluorescent, so it will emit light in a spectroscopic experiment. It has six functional groups which are all nucleophilic and capable of participating in reactions with other molecules. Catalytic rates for this reaction depend on concentration and temperature, as well as the number of chlorine atoms and polydentate ligands present in solution.</p>Formula:C8H7NO4Purity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:181.15 g/mol3-Methoxy-2-nitrobenzaldehyde
CAS:Formula:C8H7NO4Purity:98%Color and Shape:Solid, CrystallineMolecular weight:181.147



