35466-86-5

Basic information

• Product Name: 2-METHOXYETHYL METHYL CARBONATE, 97
• Synonyms: 2-METHOXYETHYL METHYL CARBONATE, 97;Methyl-2-methoxyethylcarbonate;2-METHOXYETHYL METHYL CARBONATE 97%
• CAS NO: 35466-86-5
• Molecular Formula: C₅H₁₀O₄
• Molecular Weight: 134.1305
• Mol File: 35466-86-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 95 °C(Press: 82 Torr)
• Appearance: /
• Density: 1.053±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-METHOXYETHYL METHYL CARBONATE, 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXYETHYL METHYL CARBONATE, 97(35466-86-5)
• EPA Substance Registry System: 2-METHOXYETHYL METHYL CARBONATE, 97(35466-86-5)

Safety Data

• Hazardous Substances Data: 35466-86-5(Hazardous Substances Data)

Upstream product

• 109-86-4 2-methoxy-ethanol 
• 616-38-6 carbonic acid dimethyl ester 
• 75-21-8 oxirane 
• 96-49-1 [1,3]-dioxolan-2-one 
• 67-56-1 methanol 
• 79-22-1 methyl chloroformate 

Downstream Products

• 5602-96-0 methyl p-tolylcarbamate 
• 623-08-5 N-methyl-p-toluidine 
• 32382-69-7 N-(β-Methoxyaethyl)-p-toluidin 
• 99-97-8 Dimethyl-p-toluidine 
• 102-09-0 bis(phenyl) carbonate 
• 41532-81-4 2-methoxyethyl phenyl ether 
• 100-66-3 methoxybenzene 
• 67-56-1 methanol 
• 107-25-5 methoxyethene 
• 701-56-4 4-methoxy-N,N-dimethylanilne 
• 14803-72-6 methyl N-(4-methoxyphenyl)carbamate 
• 32382-72-2 4-methoxy-N-(2-methoxyethyl)aniline 
• 5961-59-1 N-methyl-N-(4-methoxyphenyl)amine 

Relevant articles and documents

PRODUCTION METHOD OF ASYMMETRIC CHAIN CARBONATE

A method for producing an asymmetric chain carbonate by reacting an alcohol with a halocarbonate ester compound in the presence of a basic magnesium salt.

PROCESS FOR PRODUCING DIALKYL CARBONATE AND DIOL

A process for producing a dialkyl carbonate and a diol, comprising (a) subjecting a cyclic carbonate and an aliphatic monohydric alcohol to transesterification in the presence of a transesterification catalyst to produce a reaction solution containing a dialkyl carbonate and a diol, (b) extracting a dialkyl carbonate-containing reaction solution from the reaction solution and then separating a dialkyl carbonate from the dialkyl carbonate-containing reaction solution, and (c) extracting a diol-containing reaction solution from the reaction solution and then separating a diol from the diol-containing reaction solution. This process is characterized in that the content of a cyclic ether in the cyclic carbonate is 0.1 to 3,000 ppm and the content of carbonate ether in the dialkyl carbonate thus obtained is not more than 10,000 ppm.