2655-84-7

Basic information

• Product Name: 3-BROMOPHENETOLE
• Synonyms: M-BROMOPHENETOLE;3-ETHOXYBROMOBENZENE;3-BROMOPHENETOLE;3-BROMOPHENYL ETHYL ETHER;AKOS 314;1-BROMO-3-ETHOXYBENZENE;3-Bromophenetol;3-Bromophenetole,3-Bromophenyl ethyl ether
• CAS NO: 2655-84-7
• Molecular Formula: C₈H₉BrO
• Molecular Weight: 201.06
• EINECS: 220-186-9
• Product Categories: Phenetole;Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds;alkyl bromide
• Mol File: 2655-84-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 206 °C(lit.)
• Flash Point: 182 °F
• Appearance: /
• Density: 1.481 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.173mmHg at 25°C
• Refractive Index: n20/D 1.548(lit.)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-BROMOPHENETOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMOPHENETOLE(2655-84-7)
• EPA Substance Registry System: 3-BROMOPHENETOLE(2655-84-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 2655-84-7(Hazardous Substances Data)

Usage

General Description

3-Bromophenetole is a chemical compound that belongs to the organic group of substances. It has a molecular formula of C8H7BrO and is also recognized by its systematic name of 1-bromo-2-ethoxybenzene. 3-BROMOPHENETOLE appears as a clear light yellow liquid and has been used in various fields such as synthetic chemistry, pharmaceuticals, and agrochemicals for its distinctive properties. It is characterized by a strong aroma and can also act as an ether, a bromo compound, and an aromatic ether. Handling and usage of 3-Bromophenetole should be done with requisite safety measures due to its potentially harmful side effects, including eye and skin irritation.

InChI:InChI=1/C8H9BrO/c1-2-10-8-5-3-4-7(9)6-8/h3-6H,2H2,1H3

Upstream product

• 64-67-5 diethyl sulfate 
• 591-20-8 3-Bromophenol 
• 592-55-2 2-Bromoethyl ethyl ether 
• 585-79-5 m-nitrobromobenzene 
• 141-52-6 sodium ethanolate 
• 89598-96-9 (3-bromophenyl)boronic acid 
• 64-17-5 ethanol 
• 74-96-4 ethyl bromide 
• 75-03-6 ethyl iodide 
• 591-19-5 m-Bromoaniline 

Downstream Products

• 1333896-49-3 4-(3-ethoxyphenyl)-3,5-dimethylisoxazole 
• 26018-78-0 6-Aethoxybenzothiophen 
• 591-20-8 3-Bromophenol 
• 1073339-03-3 2-(3-bromo-5-ethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 54852-73-2 3-ethoxybiphenyl 
• 716359-47-6 t-butyl 4-(1-cyano-2-ethoxy-2-oxoethyl)-4-(3-ethoxyphenyl)piperidine-1-carboxylate. 
• 219706-48-6 (3-ethoxyphenyl)magnesium bromide 

Relevant articles and documents

ARYL AND HETEROARYL COMPOUNDS, AND THERAPEUTIC USES THEREOF IN CONDITIONS ASSOCIATED WITH THE ALTERATION OF THE ACTIVITY OF GALACTOCEREBROSIDASE

The application is directed to compounds of formulae (IA) and (IB): (IA) and (IB), and their salts and solvates, wherein R1a, R2a, A1, A2, A3, A4, R1b, R2b, B1, B2, B3, and G are as set forth in the specification, as well as to methods for their preparation, pharmaceutical compositions comprising the same, and use thereof for the treatment and/or prevention of, e.g., lysosomal storage diseases, such as Krabbe's disease, and α-synucleinopathies, such as Parkinson's disease.

Base Mediated Synthesis of Alkyl-aryl Ethers from the Reaction of Aliphatic Alcohols and Unsymmetric Diaryliodonium Salts

The base mediated coupling of aliphatic alcohol pronucleophiles with unsymmetric diaryliodonium salt electrophiles is described. This metal-free reaction is operationally simple, proceeds at mild temperature, and displays broad substrate scope to generate industrially important alkyl-aryl ethers in moderate to excellent yield. The synthetic utility of these reactions is demonstrated, and aspects of sustainability are highlighted by the use of unsymmetric aryl(mesityl)iodonium arylating reagents.

DIMESYLATE SALTS OF NEUROPEPTIDE Y LIGANDS

The dimesylate salt of cis-1-(3-ethoxyphenyl)-1-(4-phenylpiperazin-1-yl)4-methyl-cyclohexane has superior properties and is useful to treat physiological disorders associated with an excess of neuropeptide Y.