The chemical substance known as 4-{(1Z)-4-chloro-1-[4-(2-hydroxyethoxy)phenyl]-2-phenylbut-1-en-1-yl}phenol, with the CAS number 128585-01-3, is a complex organic compound characterized by its multi-functional structure. It features a phenolic group, which contributes to its potential as an antioxidant and its reactivity in various chemical processes. The presence of a chloro substituent indicates potential for electrophilic reactions, while the hydroxyethoxy group enhances solubility in polar solvents and may influence biological activity. The compound's conjugated double bond system suggests it may exhibit interesting optical properties and reactivity, making it a candidate for applications in pharmaceuticals or materials science. Additionally, the presence of multiple aromatic rings may contribute to its stability and interaction with biological systems. Overall, this compound's unique structural features suggest it could have diverse applications, particularly in medicinal chemistry or as a functional material.

4-{(1Z)-4-chloro-1-[4-(2-hydroxyethoxy)phenyl]-2-phenylbut-1-en-1-yl}phenol

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Ospemifene impurity is a synthetic molecule that is insoluble in water, organic solvents, and oils. It is soluble in polar solvents such as propanediol and trifluoromethyl group. Ospemifene impurity has been shown to have a high affinity for serine proteases and has been used in the immobilization of enzymes on metal surfaces.

4-Hydroxy ospemifene (ospemifene impurity)

Applications 4-Hydroxy Ospemifene is an Ospemifene (O703000) impurity, used to treat dyspareunia. It is a selective estrogen receptor modulator (SERM) acting similarly to an estrogen.
References Rutanen, E., et al.: Menopause, 10, 433 (2003);


CAS 128585-01-3: 4-{(1Z)-4-chloro-1-[4-(2-hydroxyethoxy)phenyl]-2-phenylbut-1-en-1-yl}phenol

4-Hydroxy ospemifene (ospemifene impurity)

Ref: 3D-DFA58501

4-Hydroxy Ospemifene (Ospemifene Impurity)

Ref: TR-H950140