13460-51-0 Usage
Uses
Used in Organic Synthesis:
Trihydroxyboroxine is used as a reagent in organic synthesis for its ability to facilitate a range of chemical reactions, contributing to the formation of complex organic molecules.
Used as a Boron Source:
In the production of icosahedral boranes, Trihydroxyboroxine serves as an essential boron source, playing a critical role in the synthesis of these important compounds with unique structural and chemical properties.
Used in the Synthesis of Boron-Containing Polymers and Materials:
Trihydroxyboroxine is utilized as a key building block in the creation of boron-containing polymers and materials, which have potential applications in various fields due to their distinct properties.
Used in Medicine:
Trihydroxyboroxine has potential applications in the medical field, where its unique chemical properties could be harnessed for the development of new pharmaceuticals or therapeutic agents.
Used in Agriculture:
Trihydroxyboroxine may also find use in agricultural applications, potentially contributing to the development of new agrochemicals or enhancing crop protection and yield.
Used in Materials Science:
In the realm of materials science, Trihydroxyboroxine's unique structural features could be employed in the design and synthesis of advanced materials with specific properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 13460-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,6 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13460-51:
(7*1)+(6*3)+(5*4)+(4*6)+(3*0)+(2*5)+(1*1)=80
80 % 10 = 0
So 13460-51-0 is a valid CAS Registry Number.
InChI:InChI=1/B3H3O6/c4-1-7-2(5)9-3(6)8-1/h4-6H
13460-51-0Relevant academic research and scientific papers
Vineyard,Godt Jr.
, p. 1144 - 1147 (1964)
The reaction of boric acid with amines has been found to yield either N-substituted ammonium triborates or N-substituted ammonium pentaborates. The major factors governing which product is formed are the steric requirements of the amine and the mole ratio of the reactants. Evidence is presented for the proposed structure of these products.
X-ray diffraction and micro-raman study of structural transformations in (B2O3)1-x(H2O)x glasses and liquids
Bruening, Ralf,Galbraith, Justine B.,Braedley, Katherine E.,Johnstone, Jonathan,Robichaud, Jacques,Balaji, Subramanian,Djaoued, Yahia
, p. 3745 - 3751 (2011/02/16)
Liquid water and vitreous B2O3 are the endpoints of a continuous range of random networks in which hydrogen bonds gradually replace covalent bonds. Previous work has shown that glasses can be obtained by quenching in the range x≤0.50. We report the wide-angle X-ray scattering by the liquid phase in the composition range from x=0.38 to 1.00 (pure water) at temperatures just above the liquidus. The first sharp diffraction peak (FSDP) remains at an approximately constant position in the range 0≤x≤0.8. Beyond this range, the position of the FSDP shifts linearly to higher angles. The relative concentration of the molecular species in the glasses and melts were measured with micro-Raman spectroscopy. Small molecular species are found for glasses and liquids with x;gt&0.36, determining the critical point at which the sample ceases to be a single macromolecule. Molecular water is present in liquids with x;>0.62.
