4542-75-0

Usage

Uses

Used in Plastic and Resin Products:
4,4'-BIS(BROMOMETHYL)-DIPHENYL ETHER is used as a flame retardant for enhancing the fire resistance of various plastic and resin products, providing a crucial safety feature in industries where materials are exposed to potential fire hazards.
Used in Electrical and Electronic Equipment:
In the electrical and electronic industry, 4,4'-BIS(BROMOMETHYL)-DIPHENYL ETHER is utilized as a flame retardant to improve the safety of equipment by reducing the risk of fire during operation or in the event of a malfunction.
However, it is important to note that due to concerns regarding the potential health and environmental impacts of 4,4'-BIS(BROMOMETHYL)-DIPHENYL ETHER, some regulatory restrictions have been imposed on its use in certain regions. These restrictions aim to balance the need for flame retardancy with the protection of human health and the environment.

InChI:InChI=1/C14H12Br2O/c15-9-11-1-5-13(6-2-11)17-14-7-3-12(10-16)4-8-14/h1-8H,9-10H2

Upstream product

• 1579-40-4 1,1'-oxybis(4-methyl-benzene) 
• 2350-43-8 4,4'-oxy-bis(4,1-phenylene) dimethanol 
• 14387-30-5 dimethyl 4,4'-oxydibenzoate 

Downstream Products

• 2416-40-2 4,4'-oxydibenzenemethanol diacetate 
• 71868-15-0 2-hydroxy-1-{4-[4-(2-hydroxy-2-methylpropionyl)phenoxy]phenyl}-2-methyl-propan-1-one 
• 32808-31-4 methyl 4,4'-oxybis 

Relevant academic research and scientific papers

Synthesis of bis-4H-furo[3,4-b]indoles

We describe the synthesis of two novel bis-4H-furo[3,4-b]indoles from indole. Several alternative pathways to these potential DNA bis-intercalator precursors are discussed, and the synthesis of a novel semi-rigid tether is reported.

PROCESS FOR PREPARING ARYL KETONE

A process for preparing aryl ketones is disclosed. The process includes photo-oxidizing a compound of formula (V), (VI), (VII) or (VIII): in the presence of an oxidative system comprising at least one bromide compound to form aryl ketones. X1, X2, R1, R2, R3, L1, L2, L3, L4, t, n, m and p have the meanings as described in the specification and claims.

Rotaxanes from tetralactams

Attempts to incorporate a tetralactam (3a) into a side-chain polyrotaxane by formation of its complex with p-tritylphenolate and reaction with poly(vinybenzyl chloride) failed, probably due to steric hindrance. However, three new small molecule model rota

Self-Assembled Nanotubes that Reversibly Bind Acetic Acid Guests

A large bis-urea macrocycle was synthesized and assembled into columnar nanotubes containing a sizable cavity. This purely organic nanotube is held together primarily by hydrogen bonding and yet shows remarkable thermal stability up to 180 °C in the prese

Strong binding of alkylguanidinium ions by molecular tweezers: An artificial selective arginine receptor molecule with a biomimetic recognition pattern

Bisphosphonates 2 and 3 represent the first artificial receptor molecules for alkylguanidinium ions. They bind to the guanidinium moiety by forming a 1:l chelate complex, stabilized by a planar network of electrostatic interactions and hydrogen bonds. Thi