1-Benzyl-1H-pyrazole-4-carbonitrile is an organic compound characterized by its pyrazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. The presence of a benzyl group at the 1-position and a cyano group at the 4-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic benzyl moiety. It is often studied for its potential biological activities, including anti-inflammatory and anticancer properties, making it of interest in medicinal chemistry. The cyano group enhances its reactivity, allowing for further chemical modifications. Additionally, the compound's structure suggests potential for hydrogen bonding and π-π interactions, which can influence its behavior in various chemical environments. As with many pyrazole derivatives, it may also exhibit interesting electronic properties, making it a candidate for applications in materials science and pharmaceuticals. Safety data should be consulted for handling and usage, as with all chemical substances.

1-benzyl-1H-pyrazole-4-carbonitrile

121358-86-9: 1-Benzyl-1H-pyrazole-4-carbonitrile is an organic compound characterized by its pyrazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. The presence of a benzyl group at the 1-position and a cyano group at the 4-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic benzyl moiety. It is often studied for its potential biological activities, including anti-inflammatory and anticancer properties, making it of interest in medicinal chemistry. The cyano group enhances its reactivity, allowing for further chemical modifications. Additionally, the compound's structure suggests potential for hydrogen bonding and π-π interactions, which can influence its behavior in various chemical environments. As with many pyrazole derivatives, it may also exhibit interesting electronic properties, making it a candidate for applications in materials science and pharmaceuticals. Safety data should be consulted for handling and usage, as with all chemical substances.

CAS 121358-86-9

1-benzyl-1H-pyrazole-4-carbonitrile

1-Benzyl-1H-pyrazole-4-carbonitrile

Ref: IN-DA007QHI

1-Benzyl-1H-pyrazole-4-carbonitrile

Ref: 54-OR961625

1-Benzyl-4-cyanopyrazole

Ref: 10-F048287