6705-50-6 Usage
Description
7-Oxabicyclo[2.2.1]hept-2-ene, also known as 7-Oxanorbornene, is a chemical compound that features a unique bicyclic structure with an oxygen atom incorporated into the ring. This molecule is known for its potential applications in the synthesis of various complex organic compounds and materials.
Uses
Used in Organic Synthesis:
7-Oxabicyclo[2.2.1]hept-2-ene is used as a reactant or reagent in the preparation of cyclometalated arylpyridine, arylquinoline, and arylphenanthridine complexes of iridium and platinum. These complexes serve as phosphorescent emitters, which are crucial components in the development of organic electroluminescent devices.
Used in Organic Electroluminescent Devices:
In the field of organic electroluminescent devices, 7-Oxabicyclo[2.2.1]hept-2-ene plays a significant role as a precursor for the synthesis of phosphorescent emitters. These emitters are essential for the creation of highly efficient and long-lasting light-emitting diodes (OLEDs) used in various applications such as displays, lighting, and sensors. The unique properties of 7-Oxanorbornene contribute to the enhanced performance and durability of these devices.
Check Digit Verification of cas no
The CAS Registry Mumber 6705-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6705-50:
(6*6)+(5*7)+(4*0)+(3*5)+(2*5)+(1*0)=96
96 % 10 = 6
So 6705-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O/c1-2-6-4-3-5(1)7-6/h1-2,5-6H,3-4H2
6705-50-6Relevant articles and documents
Herbicidal oxabicyclo ethers
-
, (2008/06/13)
The present invention relates to novel oxabicyclo ether derivative compounds, compositions containing these ether derivative compounds, and methods of using these compounds or compositions to control the growth of undesired vegetation. More particularly, the present invention relates to a variety of compounds, compositions, and methods of using them which are herbicidally active on a wide variety of weed species and exhibit safety to rice, cereals or broadleaf crops.
1,2-Thiazines and Related Heterocycles. Part 1. An Investigation of the Cycloadditions of N-Sulphinylanilines with 1,4-Epoxy-1,4-dihydronaphthalene and Other Alkenes
Hanson, Peter,Lewis, Robin J.,Stone, Thomas W.
, p. 1719 - 1724 (2007/10/02)
Evidence is adduced from the character of the alkenes which cycloadd to N-sulphinylanilines and from a kinetic investigation of the reactions of N-sulphinylanilines with 1,4-epoxy-1,4-dihydronaphthalene, examining the effects upon reaction rate of solvent polarity, temperature, and substitution in the N-sulphinylanilines, that the cycloadditions are pericyclic reactions of Diels-Alder type with inverse electron demand.A degree of charge separation in the transition state is indicated but this is small and confined essentially to the sulphinylaniline moiety.