19118-85-5 Usage
Uses
Used in Pharmaceutical Industry:
[1,3,2]DIOXABORINAN-2-OL is used as a reagent in organic synthesis for the development of pharmaceutical compounds. Its unique structure and properties allow for the creation of novel boron-containing molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, [1,3,2]DIOXABORINAN-2-OL is utilized as a building block for the preparation of various boron-containing compounds. These compounds can be employed in the development of new pesticides, herbicides, and other agrochemical products to enhance crop protection and yield.
Used in Materials Science:
[1,3,2]DIOXABORINAN-2-OL is used as a key component in the formation of boron-containing polymers. These polymers exhibit unique properties, such as enhanced thermal stability and mechanical strength, making them suitable for a wide range of applications in materials science, including the development of advanced composites and coatings.
Used as a Catalyst in Organic Reactions:
[1,3,2]DIOXABORINAN-2-OL is also employed as a catalyst in various organic reactions. Its ability to facilitate specific chemical transformations makes it a valuable tool in the synthesis of complex organic molecules, contributing to the advancement of organic chemistry and the development of new compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 19118-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,1 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19118-85:
(7*1)+(6*9)+(5*1)+(4*1)+(3*8)+(2*8)+(1*5)=115
115 % 10 = 5
So 19118-85-5 is a valid CAS Registry Number.
19118-85-5Relevant articles and documents
A new catalytic method for the synthesis of boroxanes
Walkowiak, Jdrzej,Marciniec, Bogdan
supporting information; experimental part, p. 6177 - 6180 (2011/01/04)
A new Ru-H complex catalyzed O-borylation of boronic acids with vinylboronates leading to boroxane bond formation with evolution of ethylene is described. Under the optimum conditions, when [Ru(CO)Cl(H)(PPh3) 3] and excess vinylboron
