1,4-Benzenedicarboxaldehyde, 2-nitro- is an organic compound characterized by the presence of two aldehyde functional groups and a nitro group attached to a benzene ring. Its molecular structure consists of a benzene core with two carboxaldehyde (-CHO) groups located at the 1 and 4 positions, and a nitro group (-NO2) at the 2 position, which contributes to its reactivity and potential applications in organic synthesis. This compound is typically a solid at room temperature and may exhibit a pale yellow to brown color. It is soluble in organic solvents, such as ethanol and acetone, but has limited solubility in water due to its hydrophobic aromatic structure. The presence of both aldehyde and nitro groups makes it a versatile intermediate in the synthesis of various chemical compounds, including pharmaceuticals and agrochemicals. Safety precautions should be taken when handling this substance, as it may pose health risks, including irritation to the skin and respiratory system.

1,4-Benzenedicarboxaldehyde, 2-nitro-

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2-nitroterephthalaldehyde

2-Nitroterephthalaldehyde is a chiral molecule that can be used in the supramolecular synthesis of macrocycles. This molecule has been shown to catalyze the formation of imines, which are important for the synthesis of macrocycles. The kinetic and thermodynamic properties of 2-Nitroterephthalaldehyde have been studied and found to be favorable for this type of reaction.

CAS 39909-72-3: 1,4-Benzenedicarboxaldehyde, 2-nitro-

2-nitroterephthalaldehyde

Ref: 10-F375453

2-Nitroterephthalaldehyde

Ref: 3D-FN133686