(3,5-Diphenyl-1H-pyrazol-1-yl)acetate, identified by its CAS number 93323-67-2, is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features two phenyl groups attached to the pyrazole ring at the 3 and 5 positions, contributing to its aromatic character and potentially influencing its chemical reactivity and solubility. The acetate functional group, derived from acetic acid, is attached to the nitrogen of the pyrazole, which can affect the compound's polarity and interaction with biological systems. Generally, compounds of this type may exhibit interesting biological activities, making them of interest in medicinal chemistry. The presence of multiple aromatic rings often suggests potential for π-π stacking interactions, which can be relevant in drug design and molecular recognition processes. Additionally, the compound's stability, solubility, and reactivity can be influenced by the substituents on the pyrazole and the acetate group, making it a versatile candidate for various applications in organic synthesis and pharmacology.

(3,5-diphenyl-1H-pyrazol-1-yl)acetate

93323-67-2: (3,5-Diphenyl-1H-pyrazol-1-yl)acetate, identified by its CAS number 93323-67-2, is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features two phenyl groups attached to the pyrazole ring at the 3 and 5 positions, contributing to its aromatic character and potentially influencing its chemical reactivity and solubility. The acetate functional group, derived from acetic acid, is attached to the nitrogen of the pyrazole, which can affect the compound's polarity and interaction with biological systems. Generally, compounds of this type may exhibit interesting biological activities, making them of interest in medicinal chemistry. The presence of multiple aromatic rings often suggests potential for π-π stacking interactions, which can be relevant in drug design and molecular recognition processes. Additionally, the compound's stability, solubility, and reactivity can be influenced by the substituents on the pyrazole and the acetate group, making it a versatile candidate for various applications in organic synthesis and pharmacology.

CAS 93323-67-2

(3,5-diphenyl-1H-pyrazol-1-yl)acetate

(3,5-Diphenyl-1h-pyrazol-1-yl)acetic acid

Ref: IN-DA0064BD

2-(3,5-Diphenyl-1H-pyrazol-1-yl)acetic acid

Ref: 54-OR1039320

(3,5-Diphenyl-pyrazol-1-yl)-acetic acid

Ref: 10-F028940