7037-28-7

Basic information

• Product Name: 2-[2-(2-morpholin-4-yl-ethoxy)-ethoxy]-ethanol
• Synonyms: 2-[2-(2-morpholin-4-yl-ethoxy)-ethoxy]-ethanol
• CAS NO: 7037-28-7
• Molecular Weight: 219.281
• Mol File: 7037-28-7.mol

Chemical Properties

• CAS DataBase Reference: 2-[2-(2-morpholin-4-yl-ethoxy)-ethoxy]-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[2-(2-morpholin-4-yl-ethoxy)-ethoxy]-ethanol(7037-28-7)
• EPA Substance Registry System: 2-[2-(2-morpholin-4-yl-ethoxy)-ethoxy]-ethanol(7037-28-7)

Safety Data

• Hazardous Substances Data: 7037-28-7(Hazardous Substances Data)

Usage

Appearance

Clear, colorless liquid

Odor

Slightly sweet

Usage

Solvent in industries like pharmaceuticals, agrochemicals, and coatings; intermediate in the synthesis of other chemical compounds

Potential applications

Surfactant, emulsifier, and dispersant

Amphiphilic nature

Ability to lower the surface tension of liquids

Safety precautions

Can be harmful if swallowed, inhaled, or absorbed through the skin

Upstream product

• 85971-96-6 3,6,12-trioxa-9-azatetradecane-1,14-diol 
• 112-27-6 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 
• 110-91-8 morpholine 
• 77544-68-4 8-tosyloxy-3,6-dioxaoctanol 

Downstream Products

• 1610450-62-8 3-methoxy-5-(2-(2-(2-morpholinoethoxy)ethoxy)ethoxy)aniline 
• 1610449-88-1 1-(3-(tert-butyl)-1-(p-tolyl)-1H-pyrazol-5-yl)-3-(4-((2-((3-methoxy-5-(2-(2-(2-morpholinoethoxy)ethoxy)ethoxy)phenyl)amino)pyrimidin-4-yl)oxy)naphthalen-1-yl)urea 
• 1610450-61-7 4-(2-(2-(2-(3-methoxy-5-nitrophenoxy)ethoxy)ethoxy)ethyl)morpholine 

Relevant articles and documents

SILICON PHTHALOCYANINE COMPLEX, PREPARATION METHOD AND MEDICINAL APPLICATION THEREOF

The present invention relates to a silicon phthalocyanine complex, the preparation method and the medicinal application thereof. The present invention particularly relates to a silicon phthalocyanine complex of formula (I), the preparation method thereof and a pharmaceutical composition comprising the same, as well as the use thereof as a photosensitizer, in particular the use in the treatment of cancers, wherein each substituent in formula (I) is the same as defined in the description.

INTRAMOLECULAR CYCLIZATION OF N,N-Di(OLIGOOXYETHYLENE)AMINES: A NEW SYNTHESIS OF MONOAZA CROWN ETHERS

The reaction of N,N-di(oligooxyethylene)amines with arenesulfonyl chloride in the presence of alkali metal hydroxide was investigated.It was found that the monoarenesulfonates of N,N-di(oligooxyethylene)amines were first formed as intermediates, and their subsequent intramolecular cyclization gave N-unsubstituted monoaza crown ethers rather selectively.