2539-21-1

Basic information

• Product Name: o-(1-methylethoxy)anisole
• Synonyms: o-(1-methylethoxy)anisole;1-Methoxy-2-(1-methylethoxy)benzene;1-Methoxy-2-isopropoxybenzene;1-isopropoxy-2-methoxybenzene
• CAS NO: 2539-21-1
• Molecular Formula: C₁₀H₁₄O₂
• Molecular Weight: 166.21696
• EINECS: 219-811-8
• Mol File: 2539-21-1.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 214.4°C at 760 mmHg
• Flash Point: 70.9°C
• Appearance: /
• Density: 0.973g/cm³
• Vapor Pressure: 0.228mmHg at 25°C
• Refractive Index: 1.483
• CAS DataBase Reference: o-(1-methylethoxy)anisole(CAS DataBase Reference)
• NIST Chemistry Reference: o-(1-methylethoxy)anisole(2539-21-1)
• EPA Substance Registry System: o-(1-methylethoxy)anisole(2539-21-1)

Safety Data

• Hazardous Substances Data: 2539-21-1(Hazardous Substances Data)

Usage

General Description

O-(1-methylethoxy)anisole, also known as 2-methoxy-4-(1-methylethoxy)toluene, is a chemical compound with the molecular formula C10H14O2. It is a colorless to pale yellow liquid with a sweet, floral odor. O-(1-methylethoxy)anisole is commonly used as a fragrance ingredient in various consumer products, such as perfumes, cosmetics, and personal care products. It is also utilized as a flavoring agent in the food industry. Additionally, this compound has potential applications in the pharmaceutical and chemical industries. Due to its pleasant odor and versatile properties, O-(1-methylethoxy)anisole is a valuable ingredient in many commercial products. However, it is important to handle this chemical with caution, as it may pose certain health and safety risks if not used properly.

InChI:InChI=1/C10H14O2/c1-8(2)12-10-7-5-4-6-9(10)11-3/h4-8H,1-3H3

Upstream product

• 75-30-9 2-iodo-propane 
• 90-05-1 2-methoxy-phenol 
• 91-16-7 1,2-dimethoxybenzene 
• 75-26-3 isopropyl bromide 
• 67-63-0 isopropyl alcohol 

Downstream Products

• 4812-20-8 2-Isopropoxyphenol 
• 36160-54-0 2-isopropyloxy-1-methoxy-4-nitrobenzene 
• 100201-00-1 1-isopropoxy-2-methoxy-4-nitro-benzene 
• 303-38-8 2,3-Dihydroxybenzoic acid 
• 85686-10-8 2-isopropoxy-3-methoxybenzoic acid 
• 85747-57-5 3-isopropoxy-2-methoxybenzoic acid 
• 30778-82-6 2-Isopropoxy-1-methoxycyclohexa-1.4-dien 
• 90-05-1 2-methoxy-phenol 
• 350685-31-3 4-Iodo-2-i-propoxyanisole 
• 596788-61-3 1,2-diiodo-4-isopropoxy-5-methoxy-benzene 
• 288387-66-6 4,5-diiodo-2-methoxyphenol 
• 269086-09-1 4,5-diethynyl-2-methoxyphenol 
• 288387-67-7 4,5-bis[(trimethylsilyl)ethynyl]-2-methoxyphenol 
• 86636-09-1 3,5-Dinitro-benzoic acid 2-isopropoxy-phenyl ester 

Relevant articles and documents

Catalytic transfer hydrogenation/hydrogenolysis of guaiacol to cyclohexane over bimetallic RuRe/C catalysts

The hydrodeoxygenation of lignin monomer guaiacol via catalytic transfer hydrogenation was studied with 2-propanol as a hydrogen donor and Ru-based catalysts. Guaiacol was mainly converted into a partially deoxygenated product, cyclohexanol (>?70% selectivity), over Ru/C catalysts with the hydrogen produced in-situ from 2-propanol. An addition of Re to Ru/C catalysts significantly enhanced the rate of C—O hydrogenolysis, resulting in the complete deoxygenation to cyclohexane (~?60% selectivity). The remarkable deoxygenation ability of the bimetallic RuRe/C catalyst is attributed to its bifunctional characteristic, by which Ru catalyzes the hydrogenation-hydrogenolysis of guaiacol and Re provides acid sites to promote cyclohexane production via hydrogenolysis.

NOVEL 3-AMINOALKYL-1,3-DIHYDRO-2H-INDOL-2-ONE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF

The present invention relates to novel 3-aminoalkyl-1,3-dihydro-2H-indol-2-one derivatives, to their preparation and to their therapeutic application. The compounds of the present invention correspond to the formula (I): in which the variables are as set forth in the specification. These compounds exhibit a strong affinity and a high selectivity for human arginine-vasopressin (AVP) V1a receptors and some compounds additionally exhibit a strong affinity for AVP V1b receptors.

Isopropoxy as a masked hydroxy group in aryl oxidative coupling reactions

Mono- and dihydroxy substituted triphenylenes have been prepared in a one-pot biphenyl/phenyl oxidative coupling reaction, in which isopropoxy acts as a masking/protecting group.