80992-57-0 Usage
Uses
Used in Organic Synthesis:
Phosphine oxide, [(1E)-1-methoxy-1-propenyl]diphenylis utilized as a reagent in organic synthesis, contributing to the formation of various complex molecules and compounds. Its role in this process is crucial for the development of new pharmaceuticals, materials, and other chemical products.
Used in Catalysis:
In the field of catalysis, phosphine oxide, [(1E)-1-methoxy-1-propenyl]diphenylserves as a ligand, enhancing the efficiency of catalytic reactions. Its ability to stabilize metal complexes is particularly beneficial in this application, allowing for more controlled and selective transformations.
Used in Materials Science:
Phosphine oxide, [(1E)-1-methoxy-1-propenyl]diphenylis explored for its potential applications in materials science, where it could contribute to the development of new materials with unique properties. Its photoactivity and interaction with metal complexes make it a promising candidate for use in advanced materials.
Used in Photoactive Compounds:
As a photoactive compound, phosphine oxide, [(1E)-1-methoxy-1-propenyl]diphenylis studied for its potential use in light-sensitive applications, such as in the development of new types of sensors or in photovoltaic technologies. Its ability to respond to light could lead to innovative applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 80992-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,9 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80992-57:
(7*8)+(6*0)+(5*9)+(4*9)+(3*2)+(2*5)+(1*7)=160
160 % 10 = 0
So 80992-57-0 is a valid CAS Registry Number.
80992-57-0Relevant academic research and scientific papers
REGIOCHEMISTRY OF REACTIONS OF α-ALKOXYALLYLPHOSPHINE OXIDE YLIDES WITH ELECTROPHILES.
Maleki, Mehran,Miller, J. Allen,Lever, O. William
, p. 3789 - 3792 (2007/10/02)
Anions 4, derived from α-methoxyallylphosphine oxides 3, react with electrophiles in a highly regioselective fashion to give products of α-attack or γ-attack depending upon the substitution pattern of the ylid 4 and the nature of the electrophile.
