2932-96-9 Usage
Uses
Used in Organic Synthesis:
(2-aminoethyl)boronic acid is used as a reagent in organic synthesis for the selective binding and reversible covalent modification of diol-containing biomolecules, enabling the development of new chemical entities and facilitating targeted reactions.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (2-aminoethyl)boronic acid is used as a key component in the development of boron-based pharmaceuticals, leveraging its unique chemical properties to create innovative therapeutic agents.
Used in Polymer Science:
(2-aminoethyl)boronic acid is utilized as a component in the preparation of boron-containing polymers, contributing to the advancement of materials with specialized properties and potential applications in various industries.
Used in Cancer Therapy:
(2-aminoethyl)boronic acid is studied for its potential as a therapeutic agent for the treatment of cancer, due to its ability to inhibit proteasome function, a crucial process in the regulation of cell cycle and apoptosis, offering a promising avenue for cancer treatment.
Used in Diabetes Management:
Additionally, (2-aminoethyl)boronic acid has been investigated for its potential role in the treatment of diabetes, as it can regulate glucose homeostasis, a critical factor in managing blood sugar levels and overall metabolic health.
Check Digit Verification of cas no
The CAS Registry Mumber 2932-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2932-96:
(6*2)+(5*9)+(4*3)+(3*2)+(2*9)+(1*6)=99
99 % 10 = 9
So 2932-96-9 is a valid CAS Registry Number.
2932-96-9Relevant academic research and scientific papers
Synthesis and NMR properties of derivatives of 5,6-dihydroborauracil and 5,6-dihydroborathymine
Ruman, Tomasz,Dlugopolska, Karolina,Kusnierz, Anna,Rode, Wojciech
experimental part, p. 180 - 184 (2010/03/01)
Novel boron compounds, a series of 4-hydroxy-5,6-dihydroborauracil and 4-hydroxy-5,6-dihydroborathymine derivatives containing various substituents at 3-, 5- and 6-positions, is presented. The spectroscopic properties, along with analyses of NMR-controlled boron compound-alcohol and boron compound-amine interactions, proves the existence of sp3-hybridized, stable B,B-bis-methoxy-5,6-dihydroborauracils and pyridine-/n-butylamine-5,6-dihydroborauracils ate-complexes in solution.
