76115-05-4

Basic information

• Product Name: 1-(4'-methoxyphenyl)-1,2,2-triphenylethanol
• Synonyms: 1-(4'-methoxyphenyl)-1,2,2-triphenylethanol
• CAS NO: 76115-05-4
• Molecular Weight: 380.486
• Mol File: 76115-05-4.mol

Chemical Properties

• CAS DataBase Reference: 1-(4'-methoxyphenyl)-1,2,2-triphenylethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4'-methoxyphenyl)-1,2,2-triphenylethanol(76115-05-4)
• EPA Substance Registry System: 1-(4'-methoxyphenyl)-1,2,2-triphenylethanol(76115-05-4)

Safety Data

• Hazardous Substances Data: 76115-05-4(Hazardous Substances Data)

Upstream product

• 611-94-9 4-Methoxybenzophenone 
• 101-81-5 Diphenylmethane 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 1733-63-7 1,2,2-triphenylethan-1-one 
• 5152-68-1 benzhydryl sodium 

Downstream Products

• 70592-05-1 (2-(4-methoxyphenyl)ethene-1,1,2-triyl)tribenzene 
• 1471339-65-7 2-[4-(1,2,2-triphenylethenyl)phenoxy]acetic acid 
• 76115-06-5 1-(4'-hydroxyphenyl)-1,2,2-triphenylethylene 

Relevant articles and documents

AIE Fluorescent Gelators with Thermo-, Mechano-, and Vapochromic Properties

A series of aggregation-induced emission (AIE) fluorescent gelators (TPE-Cn-Chol) were synthesized by attaching tetraphenylethylene (TPE) to cholesterol through an alkyl chain. The properties of the gel, nano-/microaggregate, and condensed phas

The fabrication of helical fibers with circularly polarized luminescence via ionic linkage of binaphthol and tetraphenylethylene derivatives

Assemblies with helical fiber nanostructures were fabricated via simple ionic linkage of a cationic tetraphenylethylene derivative (TPEHexN+) and an anionic binaphthyl derivative (SBNPSO3- or RBNPSO3-

Practical synthesis of unsymmetrical tetraarylethylenes and their application for the preparation of [triphenylethylene-spacer-triphenylethylene] triads

(Chemical Equation Presented) We have demonstrated that reactions of diphenylmethyllithium with a variety of substituted benzophenones produces corresponding tertiary alcohols that are easily dehydrated, without any need for purification, to produce various unsymmetrical and symmetrical tetraarylethylenes in excellent yields. The simplicity of the method allows for the preparation of a variety of ethylenic derivatives in multigram (10-50 g) quantities with great ease. The methodology was successfully employed for the preparation of various triphenylethylene (TPE)-based triads (i.e., TPE-spacer-TPE) containing polyphenylene and fluoranyl-based spacers. The ready availability of various substituted tetraarylethylenes allowed us to shed light on the effect of substituents on the oxidation potentials (Eox) of various tetraarylethylenes. Moreover, the electronic coupling among the triphenylethylene moieties in various TPE-spacer-TPE triads was briefly probed by electrochemical and optical methods.

Studies in Potential Antifertility Agents: Part XXX - Synthesis of Substituted 1--1,2,2-triphenylethylenes

Some substituted 1--1,2,2-triphenylethylenes (55-62) have been synthesized in view of the earlier report that 1,1,2,2-tetraphenylethane basic ethers possess significant anti-implantation activity in rats Indian J.Chem., 1