635537-83-6

Basic information

• Product Name: 1,2-bis(2-propionylphenoxy)ethane
• Synonyms: 1,2-bis(2-propionylphenoxy)ethane
• CAS NO: 635537-83-6
• Molecular Weight: 326.392
• Mol File: 635537-83-6.mol

Chemical Properties

• CAS DataBase Reference: 1,2-bis(2-propionylphenoxy)ethane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis(2-propionylphenoxy)ethane(635537-83-6)
• EPA Substance Registry System: 1,2-bis(2-propionylphenoxy)ethane(635537-83-6)

Safety Data

• Hazardous Substances Data: 635537-83-6(Hazardous Substances Data)

Upstream product

• 610-99-1 1-(2-Hydroxy-phenyl)-propan-1-on 
• 106-93-4 ethylene dibromide 
• 107-06-2 1,2-dichloro-ethane 

Relevant articles and documents

Cyclization of 2-(2-bromoethoxy)-acetophenones and 5-(ω-haloalkoxy)- 1,5-dihydro-2H-pyrrol-2-ones - Formation of five- to eight-membered oxygen-containing heterocycles via intramolecular alkylation

Under basic conditions (lithium diisopropylamide or sodium hydride in THF) 2-(2-bromoethoxy)-acetophenones were transformed to 3,4-dihydro[1]benzoxepin- 5(2H)-ones (homochromanones) in high yields. The preparation of novel tetrahydropyrano[2,3-b]pyrrol-6(

An efficient synthetic strategy for geometrically pure symmetrical and unsymmetrical hydroxystilbenes via McMurry coupling

Intramolecular reductive deoxygenation of ethylenedioxy tethered symmetrical and unsymmetrical aromatic bis(carbonyl) ethers with the low-valent titanium (LVT) reagent (TiCl4-Zn-THF) yielded chromatographically separable E/Z-isomers of corresponding cyclic stilbenes which were further dealkylated to obtain geometrically pure hydroxystilbenes. The intramolecular McMurry coupling of the tethered bis(carbonyl) ethers with TiCl 3-Li-THF, on the other hand, directly provided both symmetrical and unsymmetrical phenanthrenes via in situ dealkoxylation of the phenol function. This is the first report of the synthesis of unsymmetrical phenanthrenes by the LVT route.