60835-90-7

Basic information

• Product Name: 1-bromo-4-(2-methoxyethyl)benzene
• Synonyms: 1-bromo-4-(2-methoxyethyl)benzene
• CAS NO: 60835-90-7
• Molecular Formula: C₉H₁₁BrO
• Molecular Weight: 215.08704
• Mol File: 60835-90-7.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-bromo-4-(2-methoxyethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-4-(2-methoxyethyl)benzene(60835-90-7)
• EPA Substance Registry System: 1-bromo-4-(2-methoxyethyl)benzene(60835-90-7)

Safety Data

• Hazardous Substances Data: 60835-90-7(Hazardous Substances Data)

Usage

General Description

1-bromo-4-(2-methoxyethyl)benzene is an organic compound with the chemical formula C9H11BrO. It is a colorless liquid with a characteristic odor, and it is widely used as an intermediate in the production of various pharmaceuticals, agrochemicals, and other organic compounds. The compound contains a benzene ring with a bromine atom at the 1 position and a 2-methoxyethyl group at the 4 position. It is primarily used in organic synthesis as a building block for the production of more complex chemicals. 1-bromo-4-(2-methoxyethyl)benzene is also used as a solvent and a reagent in organic reactions. It should be handled and stored with care due to its potential hazards, including its flammability and its ability to cause skin and eye irritation.

Upstream product

• 107-30-2 chloromethyl methyl ether 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 41841-16-1 (4-bromo-phenyl)-acetic acid methyl ester 
• 106-37-6 1.4-dibromobenzene 
• 67-56-1 methanol 
• 74-85-1 ethene 
• 6999-03-7 1-bromo-4-(trimethylsilyl)benzene 
• 1878-68-8 2-(4-bromophenyl)-acetic acid 
• 37859-24-8 2-(4-bromophenyl)acetyl chloride 
• 4654-39-1 4-bromophenethanol 
• 74-88-4 methyl iodide 

Downstream Products

• 60835-91-8 4-(2-methoxyethyl)benzoic acid 
• 84803-56-5 4-(2-methoxyethyl)aniline 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 1082066-32-7 2-(4-(2-methoxyethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1450816-85-9 (2E,2'E)-diethyl 3,3'-(5-(methoxycarbonyl)-2-(2-methoxyethyl)-1,3-phenylene)diacrylate 
• 1450816-84-8 (E)-methyl 3-(3-ethoxy-3-oxoprop-1-en-1-yl)-4-(2-methoxyethyl)benzoate 
• 1450816-98-4 methyl 4-(2-methoxyethyl)benzoate 
• 60835-87-2 4-(β-Methoxyethyl)-benzoesaeure-methyl-d3-ester 

Relevant articles and documents

Oxidative 1,2-Difunctionalization of Ethylene via Gold-Catalyzed Oxyarylation

Under the conditions of oxidative gold catalysis, exposure of ethylene to aryl silanes and alcohols generates products of 1,2-oxyarylation. This provides a rare example of a process that allows catalytic differential 1,2-difunctionalization of this feedstock chemical.

OXAZOLIDINONE HYDROXAMIC ACID COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS

This invention pertains generally to treating bacterial infections using organic compounds of Formula I. In certain aspects, the invention pertains to treating infections caused by Gram-negative bacteria. (I) wherein X, Y, R1, R2, R3, R4 and R5 and defined herein.

Synthesis of ethers from esters via Fe-catalyzed hydrosilylation

Triiron dodecacarbonyl allows for the selective reduction of esters into the corresponding ethers. This protocol has a wide substrate scope. In addition, cholesteryl pelarogonate has been reduced under the reaction conditions with an excellent yield.