4792-39-6

Basic information

• Product Name: 1,1-Bis(p-methoxyphenyl)propane
• CAS NO: 4792-39-6
• Molecular Formula: C₁₇H₂₀O₂
• Molecular Weight: 256.345
• Mol File: 4792-39-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 370.2°Cat760mmHg
• Flash Point: 139.5°C
• Density: 1.022g/cm³
• CAS DataBase Reference: 1,1-Bis(p-methoxyphenyl)propane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-Bis(p-methoxyphenyl)propane(4792-39-6)
• EPA Substance Registry System: 1,1-Bis(p-methoxyphenyl)propane(4792-39-6)

Safety Data

• Hazardous Substances Data: 4792-39-6(Hazardous Substances Data)

Usage

General Description

1,1-Bis(p-methoxyphenyl)propane, also known as bisphenol F, is a chemical compound used in the production of epoxy resins and polycarbonate plastics. It is derived from the reaction of acetone with two equivalents of phenol in the presence of an acid catalyst. This chemical is commonly found in consumer products such as food and beverage can linings, thermal paper, and electronics. Studies have shown that exposure to bisphenol F may have potential adverse health effects, particularly on the endocrine system, leading to concerns about its safety and regulation. As a result, there is ongoing research and monitoring of this compound to better understand its impact on human health and the environment.

Upstream product

• 123-38-6 propionaldehyde 
• 100-66-3 methoxybenzene 
• 1576-13-2 1,1-bis-(4-hydroxyphenyl)propane 
• 77-78-1 dimethyl sulfate 
• 74-88-4 methyl iodide 
• 4663-13-2 1,1-bis(4-methoxyphenyl)propene 
• 121-97-1 4-Methoxypropiophenone 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 384842-35-7 1,1-bis(4-methoxyphenyl)propanol 
• 31067-02-4 1,1-Bis(p-methoxyphenyl)ethan-1-ol 
• 90-96-0 bis(p-methoxyphenyl)methanone 
• 4356-69-8 1,1-bis-(4-methoxyphenyl)ethylene 
• 4180-23-8 E-1-(4'-methoxyphenyl)prop-1-ene 
• 7525-23-7 4,4'-dimethoxydiphenylmethyl chloride 

Downstream Products

• 4180-23-8 E-1-(4'-methoxyphenyl)prop-1-ene 
• 100-66-3 methoxybenzene 

Relevant articles and documents

Room-temperature bismuth-catalyzed bis-arylation of carbonyl compounds with aryl ethers and phenols

Using Bi2(SO4)3 as the catalyst and TMSCl as the additive, a wide variety of aldehydes, ketones, and acetals were smoothly condensed with aryl ethers at room temperature to provide the corresponding diarylmethanes and triarylmethanes selectively in good to excellent yields. Using Bi2(SO4)3 as the catalyst and TMSCl as the additive, a wide variety of aldehydes, ketones, and acetals were smoothly condensed with aryl ethers at room temperature to selectively provide the corresponding diarylmethanes and triarylmethanes in good to excellent yields. Copyright

Dual-reagent catalysis within Ir-Sn domain: Highly selective alkylation of arenes and heteroarenes with aromatic aldehydes

(Chemical Equation Presented) Reactions of arenes and heteroarenes with aromatic aldehydes proceeded smoothly in the presence of a catalytic combination of [Ir(COD)Cl]2-SnCl4 to afford the corresponding triarylmethane derivatives (TRAMs) in high yields. This 100% TRAM selective transformation is clean and eliminates the use of acid systems.

Molybdenum-catalyzed aromatic substitution with olefins and alcohols

A new type of electrophilic aromatic substitution without using organic halides has been realized by using Mo(CO)6 catalyst.