98627-35-1

Basic information

• Product Name: Benzene, 1-(2-methoxyethyl)-4-(phenylmethoxy)-
• CAS NO: 98627-35-1
• Molecular Formula: C16H18O2
• Molecular Weight: 242.318
• Mol File: 98627-35-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(2-methoxyethyl)-4-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(2-methoxyethyl)-4-(phenylmethoxy)-(98627-35-1)
• EPA Substance Registry System: Benzene, 1-(2-methoxyethyl)-4-(phenylmethoxy)-(98627-35-1)

Safety Data

• Hazardous Substances Data: 98627-35-1(Hazardous Substances Data)

Upstream product

• 61439-59-6 2-(4-benzyloxyphenyl)ethanol 
• 77-78-1 dimethyl sulfate 
• 106-48-9 4-chloro-phenol 
• 7700-27-8 4-chlorophenyl benzyl ether 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 501-94-0 p-hydroxyphenethyl alcohol 
• 74-88-4 methyl iodide 

Downstream Products

• 56718-71-9 4-(2-methoxyethyl)phenol 

Relevant articles and documents

To the methoxy ethyl phenol synthesis method (by machine translation)

The invention discloses a method for synthesizing methoxy ethyl phenol, to the chlorophenol as the starting material, through the phenolic hydroxyl protection, format reaction, methylation and hydrogenation debenzylation reaction to obtain the target product to the methoxy ethyl phenol process, the methylation reaction is just a simple filtering operation that can be used for the next step reaction, without any other operation. This invention adopts the [...] as the starting material to synthesize to methoxy ethyl phenol, reduce the difficulty of after treatment, reduce the reaction time, the product has high purity, high yield, good stability of the product. (by machine translation)

The evaluation of a biogenetically based approach to the synthesis of octahydro-1H-benzofuro[3,2-e]isoquinolines

A potential synthetic route to octahydro-1H-benzofuro[3,2-e]isoquinoline derivatives by intermolecular oxidative phenolic coupling has been studied. A variety of successful coupling reactions have been effected between 2-naphthol or 4-t-butylphenol and p-cresol, 2-(p-hydroxyphenyl)ethanol, 3,4-dimethylphenol, 5-indanol and 6-hydroxytetralin, but 2-acetyl-7-hydroxytetrahydroisoquinoline failed to participate in such reactions.