1-Phenyl-1H-pyrazole-5-carbaldehyde is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a phenyl group attached to the pyrazole ring, enhancing its aromatic properties. The presence of the aldehyde functional group (-CHO) at the 5-position of the pyrazole contributes to its reactivity, making it a potential candidate for various chemical reactions, including condensation and oxidation. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The compound is of interest in medicinal chemistry and material science due to its potential biological activities and applications in synthesizing other complex molecules. Its reactivity and structural features make it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. As with many organic compounds, handling should be done with care, considering safety protocols to mitigate any potential hazards associated with its use.

1-phenyl-1H-pyrazole-5-carbaldehyde

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1H-Pyrazole-5-carboxaldehyde, 1-phenyl-

1-Phenyl-1H-pyrazole-5-carboxaldehyde

1-Phenyl-1H-pyrazole-5-carbaldehyde (1PP) is a pyrazolyl compound that undergoes 1,3-dipolar cycloaddition to form imines. This reaction can be catalyzed by light or heat, and the tautomerization of this imine to an azomethine intermediate can be observed in experiments. The regiochemistry of the 1,3-dipolar cycloaddition is dependent on the orientation of the dipolarophile with respect to the pyrazolyl ring. It was found that 1PP reacts with aldehydes and ketones to form unsymmetrical pyrazoles in yields up to 99%.

CAS 132274-70-5: 1-phenyl-1H-pyrazole-5-carbaldehyde

1H-Pyrazole-5-carboxaldehyde, 1-phenyl-

Ref: IN-DA0010GC

1-Phenyl-1H-pyrazole-5-carboxaldehyde

Ref: 54-OR23388

1-Phenyl-1H-pyrazole-5-carbaldehyde

Ref: 3D-FP126824

1-Phenyl-1H-pyrazole-5-carbaldehyde

Ref: 10-F077334