1067-88-5 Usage
Uses
Used in Adhesives Industry:
Phosphonic acid, 1-propynyl-, diethyl ester is used as a coupling agent for improving the adhesion and compatibility between different materials in adhesive formulations. This enhances the performance and durability of adhesive products.
Used in Coatings Industry:
In the coatings industry, Phosphonic acid, 1-propynyl-, diethyl ester is used as a surface modifier to enhance the adhesion and compatibility of coatings on various substrates. This results in improved durability, corrosion resistance, and overall performance of the coatings.
Used in Sealants Industry:
Phosphonic acid, 1-propynyl-, diethyl ester is used as a coupling agent in sealant formulations to improve the adhesion and compatibility between different materials. This ensures a strong bond and better sealing performance in various applications.
Used in Pharmaceutical and Agrochemical Synthesis:
Phosphonic acid, 1-propynyl-, diethyl ester has potential applications in the synthesis of pharmaceuticals and agrochemicals, where it can be used as a building block or intermediate in the development of new compounds with desired properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1067-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1067-88:
(6*1)+(5*0)+(4*6)+(3*7)+(2*8)+(1*8)=75
75 % 10 = 5
So 1067-88-5 is a valid CAS Registry Number.
1067-88-5Relevant academic research and scientific papers
Expanding the scope of Enantioselective FerroPHANE-promoted [3+2] annulations with α,β-unsaturated ketones
Pinto, Nathalie,Neel, Mathilde,Panossian, Armen,Retailleau, Pascal,Gilles Frison,Voituriez, Arnaud,Marinetti, Angela
scheme or table, p. 1033 - 1045 (2010/05/19)
The planar chiral 2-phospha [3]ferrocenophane I has been shown to be the first efficient nucleo- philic organocatalyst for the enantiose- lective synthesis of cyclopentenyl- phosphonates, through [3+2] cycliza- tions between diethyl allenylphospho- nate a
Use of allenylphosphonates as new substrates for phosphane-catalyzed [3+2] and [4+2] annulations
Panossian, Armen,Fleury-Bregeot, Nicolas,Marinetti, Angela
scheme or table, p. 3826 - 3833 (2009/04/07)
The suitability of allenylphosphonates as substrates in phosphane-catalyzed annulation reactions has been investigated. Despite their lower reactivity relative to allenyl esters, allenylphosphonates overall display the anticipated behavior: pyrrolines, te
