2065-16-9

Basic information

• Product Name: 4-[1-[4-(2-Hydroxyethoxy)phenyl]-1-methylethyl]phenol
• Synonyms: 2-(4-Hydroxyphenyl)-2-[p-(2-hydroxyethoxy)phenyl]propane;4-[1-[4-(2-Hydroxyethoxy)phenyl]-1-methylethyl]phenol;4-[1-Methyl-1-[4-(2-hydroxyethoxy)phenyl]ethyl]phenol
• CAS NO: 2065-16-9
• Molecular Formula: C₁₇H₂₀O₃
• Molecular Weight: 272.34
• Mol File: 2065-16-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-[1-[4-(2-Hydroxyethoxy)phenyl]-1-methylethyl]phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[1-[4-(2-Hydroxyethoxy)phenyl]-1-methylethyl]phenol(2065-16-9)
• EPA Substance Registry System: 4-[1-[4-(2-Hydroxyethoxy)phenyl]-1-methylethyl]phenol(2065-16-9)

Safety Data

• Hazardous Substances Data: 2065-16-9(Hazardous Substances Data)

Upstream product

• 75-21-8 oxirane 
• 80-05-7 BPA 
• 1313878-02-2 C₁₉H₂₂O₄ 
• 107-21-1 ethylene glycol 

Downstream Products

• 901-44-0 dyanol 22 
• 1313877-89-2 C₂₀H₂₅ClO₃ 

Relevant articles and documents

BISPHENOL DERIVATIVES AND THEIR USE AS ANDROGEN RECEPTOR ACTIVITY MODULATORS

This invention provides bisphenol derivatives having a structure of formula I. Said compounds are modulators of the androgen receptor activity and are useful in the treatment of various diseases, including prostate cancer, breast cancer, ovarian cancer, endometrial cancer, acne, ovarian cysts, polycystic ovarian disease, age-related macular degeneration, precocious puberty, hirsutism and air loss.

Aromatic ethers and process for producing aromatic ethers

According to a production process, aromatic ethers are producible by reacting phenols with an oxirane compound with use of an anion exchange resin as a catalyst. According to another production process, aromatic ethers having an alcoholic hydroxyl group are producible by a crystallization-purification step of using a solvent having a solubility parameter ranging from 7.5 to 12.5 for purification by crystallization. Further, according to still another production process, producible are aromatic ethers having an alcoholic hydroxyl group, wherein the content of a metal in the aromatic ethers is less than 100 ppm by mass, and the content of a halogen element in the aromatic ethers is less than 100 ppm by mass.