54149-18-7

Basic information

• Product Name: 2-(2-methoxyethoxy)-1H-Isoindole-1,3(2H)-dione
• Synonyms: 2-(2-methoxyethoxy)-1H-Isoindole-1,3(2H)-dione;2-(2-methoxyethoxy)-2,3-dihydro-1H-isoindole-1,3-dione
• CAS NO: 54149-18-7
• Molecular Formula: C₁₁H₁₁NO₄
• Molecular Weight: 221.21
• Mol File: 54149-18-7.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-methoxyethoxy)-1H-Isoindole-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-methoxyethoxy)-1H-Isoindole-1,3(2H)-dione(54149-18-7)
• EPA Substance Registry System: 2-(2-methoxyethoxy)-1H-Isoindole-1,3(2H)-dione(54149-18-7)

Safety Data

• Hazardous Substances Data: 54149-18-7(Hazardous Substances Data)

Usage

Physical State

White solid

Solubility

Soluble in organic solvents

Industrial and Research Applications

Potential use in the development of new materials such as polymers and coatings

Pharmaceutical Research

Potential building block for the synthesis of new drugs

Anti-Corrosive Agent

Potential use in the protection of metal surfaces

Potential Applications

Across different industries and research fields

Upstream product

• 524-38-9 N-hydroxyphthalimide 
• 109-86-4 2-methoxy-ethanol 
• 6482-24-2 2-Bromoethyl methyl ether 
• 17178-10-8 2-methoxy-ethyl p-toluenesulfonyloxy ester 
• 4296-15-5 2-iodo-1-methoxyethane 

Downstream Products

• 54149-39-2 O-(2-Methoxy-ethyl)-hydroxylamine 
• 504436-39-9 N-[5(S)-3-[3-fluoro-4-[(1α,5α,6α)-6-[(2-(methoxy)ethoxyimino)methyl]-3-azabicyclo[3.1.0]hexan-3-yl]phenyl]-2-oxooxazolidin-5-ylmethyl]acetamide 
• 109-85-3 2-methoxyethylamine 
• 99522-43-7 (E)-2-(3-phenylprop-2-enyloxy)ethan-1-ol 

Relevant articles and documents

Catalytic Asymmetric Csp3?H Functionalization under Photoredox Conditions by Radical Translocation and Stereocontrolled Alkene Addition

This work demonstrates how photoredox-mediated C(sp3)?H activation through radical translocation can be combined with asymmetric catalysis. Upon irradiation with visible light, α,β-unsaturated N-acylpyrazoles react with N-alkoxyphthalimides in the presence of a rhodium-based chiral Lewis acid catalyst and the photosensitizer fac-[Ir(ppy)3] to provide a C?C bond-formation product with high enantioselectivity (up to 97 % ee) and, where applicable, with some diastereoselectivity (3.0:1 d.r.). Mechanistically, the synthetic strategy exploits a radical translocation (1,5-hydrogen transfer) from an oxygen-centered to a carbon-centered radical with a subsequent stereocontrolled radical alkene addition.

HMOX1 inducers

The present invention is related to compounds of structure (I) as heme oxygenase 1 (HMOX 1) inducers. The present invention is also related a method of controlling the activity or the amount, or both the activity and the amount, of heme-oxygenase 1 in a mammalian subject. The definitions of the variables are provided herein.

CONTROLLED RELEASE OF ACTIVE COMPOUNDS FROM DYNAMIC MIXTURES

The present invention relates to a dynamic mixture in the form of a dynamic mixture obtained by reacting together, in the presence of water, at least one O-substituted hydroxylamine or S-substituted thiohydroxylamine derivative with at least one perfuming