92988-08-4 Usage
Uses
Used in Polymer Production:
Trivinylboroxin is used as a monomer for the polymerization process, contributing to the formation of polymers with unique properties. Its incorporation enhances the adhesiveness, flexibility, and thermal stability of the resulting polymers, making them suitable for a wide range of applications.
Used in Organic Synthesis:
In the field of organic synthesis, Trivinylboroxin serves as a valuable building block. Its reactivity and structural features facilitate the synthesis of a variety of organic compounds, broadening the scope of chemical research and development.
Used as a Catalyst in Chemical Reactions:
Trivinylboroxin is employed as a catalyst to accelerate chemical reactions, improving the efficiency and selectivity of various processes. Its catalytic properties are harnessed in different industries to streamline production and enhance the quality of end products.
Used in Advanced Materials Production:
As a key component in the creation of advanced materials, Trivinylboroxin is instrumental in the fields of chemistry, materials science, and industrial manufacturing. Its unique properties and reactivity make it an essential ingredient in the development of innovative materials with improved performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 92988-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,8 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92988-08:
(7*9)+(6*2)+(5*9)+(4*8)+(3*8)+(2*0)+(1*8)=184
184 % 10 = 4
So 92988-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H9B3O3/c1-4-7-10-8(5-2)12-9(6-3)11-7/h4-6H,1-3H2
92988-08-4Relevant academic research and scientific papers
Reactivity of cyclic sulfamidates towards phosphonate-stabilised enolates: Synthesis and applications of α-phosphono lactams
Bower, John F.,Williams, Andrew J.,Woodward, Hannah L.,Szeto, Peter,Lawrence, Ron M.,Gallagher, Timothy
, p. 2636 - 2644 (2008/03/11)
Five and six ring α-phosphono lactams 14-20 are available by reaction of 1,2- and 1,3-cyclic sulfamidates respectively with enolates derived from ethyl dialkylphosphonoacetates 3 and 4. Subsequent Wadsworth-Emmons olefination provides the enantiomerically
The preparation of optically active boronic ester substituted Δ2-isoxazolines
Wallace, Richard H.,Zong
, p. 87 - 91 (2007/10/03)
In this paper we report our recent results in the area of nitrile oxide cycloaddition to optically active vinylboronic esters to afford optically active boronic ester substituted Δ2-isoxazolines. In these studies, a number of optically active d
