31600-56-3

Basic information

• Product Name: [(2-methoxyethoxy)methyl]benzene
• Synonyms: [(2-methoxyethoxy)methyl]benzene;(2-Methoxyethyl)benzyl ether;1-(Benzyloxy)-2-methoxyethane;2-Methoxyethylbenzyl ether
• CAS NO: 31600-56-3
• Molecular Formula: C₁₀H₁₄O₂
• Molecular Weight: 166.21696
• EINECS: 250-722-7
• Mol File: 31600-56-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 219.6°Cat760mmHg
• Flash Point: 74.4°C
• Appearance: /
• Density: 0.989g/cm³
• Vapor Pressure: 0.175mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: [(2-methoxyethoxy)methyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: [(2-methoxyethoxy)methyl]benzene(31600-56-3)
• EPA Substance Registry System: [(2-methoxyethoxy)methyl]benzene(31600-56-3)

Safety Data

• Hazardous Substances Data: 31600-56-3(Hazardous Substances Data)

Usage

General Description

[(2-methoxyethoxy)methyl]benzene, also known by its IUPAC name 1-[(2-methoxyethoxy)methyl]benzene, is a chemical compound with the molecular formula C10H14O3. It is a colorless liquid with a faint and sweet odor. [(2-methoxyethoxy)methyl]benzene is used as a solvent in various industrial applications, such as in the production of paints, coatings, and adhesives. It is also used in the synthesis of specialty chemicals and pharmaceuticals. [(2-methoxyethoxy)methyl]benzene is considered to have low toxicity and is not expected to pose significant risks to human health or the environment when properly handled and used according to safety guidelines. However, it is important to handle this chemical with care and use appropriate personal protective equipment when working with it.

InChI:InChI=1/C10H14O2/c1-11-7-8-12-9-10-5-3-2-4-6-10/h2-6H,7-9H2,1H3

Upstream product

• 109-86-4 2-methoxy-ethanol 
• 100-51-6 benzyl alcohol 
• 1327238-85-6 ((2-methoxyethoxy)methoxy)cyclohexane 
• 110-71-4 1,2-dimethoxyethane 
• 100-52-7 benzaldehyde 
• 71412-83-4 benzaldehyde di-2-methoxyethyl acetal 
• 3970-21-6 2-Methoxyethoxymethyl chloride 
• 591-51-5 phenyllithium 
• 622-08-2 2-Benzyloxyethanol 
• 74-88-4 methyl iodide 
• 100-39-0 benzyl bromide 

Downstream Products

• 109-86-4 2-methoxy-ethanol 
• 65-85-0 benzoic acid 

Relevant articles and documents

Iridium solutes effect C-H bond activation and C-C bond forming reactions of C6H6-MeOCH2CH2OMe solvent mixtures

The in situ generated [TpMe2Ir(C6H5) 2] fragment induces both aromatic and aliphatic C-H bond activation reactions, along with C-C bond formation, when heated with benzene and 1,2-dimethoxyethane.

Asymmetric epoxidation of unfunctionalized olefins catalyzed by Jacobsen's catalyst on alkoxyl-modified zirconium poly (styrene-phenylvinylphosphonate)-phosphate (ZPS-PVPA)

New chiral Jacobsen's catalysts grafted onto alkoxyl-modified ZPS-PVPA are synthesized and applied in asymmetric epoxidations of unfunctionalized olefins. Specially, the supported catalysts indicate excellent catalytic activities (conv%, up to 96; sele%, up to 96; ee%, up to >99) in the absence of N-methylmorpholine N-oxide (NMO) by virtue of the special configurations of the catalysts. The superior stability (recycling for ten times) and the comfortable dispositions in large-scale reactions (such as 200 times) grant the potential application in industry to the heterogeneous catalysts.

COMPOSITIONS, SYNTHESIS, AND METHODS OF USING PHENYLCYCLOALKYLMETHYLAMINE DERIVATIVES

The present invention provides novel phenylcycloalkylmethylamme derivatives, and methods of preparing phenylcycloalkylmethylamme derivatives. The present invention also provides methods of using phenylcycloalkylmethylamme derivatives and compositions of phenylcycloalkylmethylamme derivatives. The pharmaceutical compositions of the compounds of the present invention can be used for treating and/or preventing obesity and obesity related co- morbid indications and depression and depression related co-morbid indications.