3383-74-2

Basic information

• Product Name: 1-Methoxy-4-(2-chloroethoxy)benzene
• Synonyms: 1-Methoxy-4-(2-chloroethoxy)benzene;2-Chloroethyl(4-methoxyphenyl) ether;4-(2-Chloroethoxy)-1-methoxybenzene;1-(2-chloroethoxy)-4-methoxybenzene(SALTDATA: FREE)
• CAS NO: 3383-74-2
• Molecular Formula: C₉H₁₁ClO₂
• Molecular Weight: 186.64
• Mol File: 3383-74-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 272.657°C at 760 mmHg
• Flash Point: 107.628°C
• Appearance: /
• Density: 1.129g/cm³
• Vapor Pressure: 0.01mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: 1-Methoxy-4-(2-chloroethoxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methoxy-4-(2-chloroethoxy)benzene(3383-74-2)
• EPA Substance Registry System: 1-Methoxy-4-(2-chloroethoxy)benzene(3383-74-2)

Safety Data

• Hazardous Substances Data: 3383-74-2(Hazardous Substances Data)

Usage

General Description

1-Methoxy-4-(2-chloroethoxy)benzene is an organic chemical compound that belongs to the class of methoxybenzene and is also known as eugenyl chloride. It is a colorless to pale yellow liquid with a sweet, floral odor and is primarily used as a fragrance and flavoring agent in the food and beverage industry. It is also utilized in the production of perfumes, soaps, and cosmetics. Additionally, this compound has potential applications in the pharmaceutical industry as an intermediate in the synthesis of various drugs and pharmaceutical products. However, it is important to handle this chemical with care as it may cause skin and eye irritation upon contact.

InChI:InChI=1/C9H11ClO2/c1-11-8-2-4-9(5-3-8)12-7-6-10/h2-5H,6-7H2,1H3

Upstream product

• 3570-58-9 2-chloroethyl mesylate 
• 150-76-5 4-methoxy-phenol 
• 107-04-0 1-Bromo-2-chloroethane 
• 107-06-2 1,2-dichloro-ethane 

Downstream Products

• 114276-19-6 1-[2-(4-methoxy-phenoxy)-ethyl]-4-phenyl-piperidine-4-carboxylic acid ethyl ester 
• 101568-63-2 2-[2-(4-methoxy-phenoxy)-ethylamino]-ethanol 
• 4024-19-5 1-methoxy-4-(vinyloxy)benzene 
• 145276-56-8 6-<4-(4-methoxyphenoxyethyl)-1-piperazinyl>-3(2H)-pyridazinone 
• 25836-83-3 N-(2-(4-methoxyphenoxy)ethyl)aniline 
• 1417997-97-7 C₂₁H₂₄O₆ 
• 100238-55-9 4-(2-chloroethoxy)phenol 
• 99355-75-6 5-methoxy-2,3-dihydrobenzofuran-6-carboxaldehyde 
• 281678-65-7 1,4-dibromo-2-(2-chloro-ethoxy)-5-methoxy-benzene 
• 10450-25-6 [2-(3,4-Dimethoxy-phenyl)-ethyl]-[2-(4-methoxy-phenoxy)-ethyl]-amine 
• 10461-24-2 1-[2-(4-Methoxy-phenoxy)-ethylamino]-2-methyl-pentan-2-ol 
• 10461-57-1 1-Allyloxy-3-[2-(4-methoxy-phenoxy)-ethylamino]-propan-2-ol 

Relevant articles and documents

METHOD FOR PRODUCING POTASSIUM SALT, AND POTASSIUM SALT

PROBLEM TO BE SOLVED: To provide a method that makes it possible to efficiently produce a halogen compound useful as a precursor of a compound that can be used suitably for optical materials in general. SOLUTION: A method for producing potassium salt includes the step for producing potassium salt represented by formula (1) by the reaction between a compound represented by formula (3), a cyclic carbonate ester compound, and potassium carbonate. [R2 is an aromatic ring-containing group having C constituting an aromatic ring at a binding site to O; n is 1 or 2; R1 independently represents an alkylene group]. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

MANUFACTURING METHOD OF HALOGEN COMPOUND, MANUFACTURING METHOD OF POTASSIUM SALT AND POTASSIUM SALT

PROBLEM TO BE SOLVED: To provide a method capable of manufacturing a halogen compound useful as a precursor of a compound capable of being preferably used especially for optical system materials generally with high efficiency. SOLUTION: There is provided a manufacturing method of a halogen compound including a process of reacting a compound represented by the following formula (1) and a halogenation agent to produce a halogen compound represented by the following formula (2). In the formula (1), R1 is a linear or branched alkylene group, R2 is an aromatic ring-containing group having a carbon atom constituting an aromatic ring at a binding part with an oxygen atom represented in the formula, n is 1 or 2 and two of R1s may same or different when n is 2. In the formula (2), X is a halogen atom. COPYRIGHT: (C)2016,JPOandINPIT

A practical approach to highly functionalized benzodihydrofurans

A number of aromatic dibromides have been treated with 2-3 equivalents of n-butyllithium in order to initiate two sequential chemical events, a Parham cyclization and an intermolecular reaction with DMF. (C) 2000 Elsevier Science Ltd.