330976-39-1

Basic information

• Product Name: o-(2-Methoxyethyl)phenol
• Synonyms: 2-(2-Methoxyethyl)phenol;o-(2-Methoxyethyl)phenol
• CAS NO: 330976-39-1
• Molecular Formula: C9H12O2
• Molecular Weight: 152.19038
• Mol File: 330976-39-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: o-(2-Methoxyethyl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: o-(2-Methoxyethyl)phenol(330976-39-1)
• EPA Substance Registry System: o-(2-Methoxyethyl)phenol(330976-39-1)

Safety Data

• Hazardous Substances Data: 330976-39-1(Hazardous Substances Data)

Usage

Description

o-(2-Methoxyethyl)phenol, also known as 2-(2-Methoxyethyl)phenol, is an organic compound characterized by its hydroxyl group attached to a phenol ring with a methoxyethyl side chain. This structure endows it with specific chemical and physical properties that make it suitable for various applications, particularly as a stabilizer in the chemical industry.

Uses

Used in the Coatings Industry:
o-(2-Methoxyethyl)phenol is used as a stabilizer for the preparation of polysiloxane-based coating compounds. Its stabilizing properties contribute to the production of coatings with enhanced stability and durability, making it a valuable additive in this application.
The provided materials indicate that o-(2-Methoxyethyl)phenol is utilized specifically in the coatings industry for its stabilizing effects on polysiloxane-based compounds. There is no mention of other industries or applications in the given data, so the summary focuses solely on its use in the coatings industry.

Upstream product

• 90-02-8 salicylaldehyde 
• 1260168-27-1 2-(2-methoxyethenyl)phenol 

Relevant articles and documents

Synthesis method of metroprolol succinate ortho-isomer impurities

The invention belongs to the technical field of medicinal chemistry, and particularly relates to a synthesis method of metroprolol succinate ortho-isomer impurities. The synthesis method comprises thesteps: the metroprolol succinate ortho-isomer impurities are prepared by taking salicylaldehyde as a raw material through four steps of reactions, namely the Wittig reaction, the reduction hydrogenation reaction, the substitution reaction and the ring-opening reaction. The synthesis method of the metroprolol succinate ortho-isomer impurities totally includes the four steps of reactions, the raw material is easy to obtain, the total yield is greater than 40%, and contribution is made to strictly control the content of the metroprolol succinate ortho-isomer impurities through an external standard method; and the synthesis method of the metroprolol succinate ortho-isomer impurities is easy to operate, mild in reaction, high in product purity and suitable for drug quality study.

Multidentate phosphite ligands, catalytic compositions containing such ligands, and catalytic prosses utilizing such catalytic compositions

Multidentate phosphite ligands are disclosed for use in reactions such as hydrocyanation and isomerization. The catalyst compositions made therefrom and the various catalytic processes which employ such multidentate phosphite ligands are also disclosed. I