863753-30-4 Usage
Description
(2-Aminophenyl)boronic acid hydrochloride is an organic compound that features a boron atom bonded to an aromatic ring with an amino group attached to the ortho position. (2-Aminophenyl)boronic acid hydrochloride is known for its unique chemical properties, such as its ability to form stable covalent bonds with diols and its potential to act as a Lewis acid.
Uses
Used in Pharmaceutical Industry:
(2-Aminophenyl)boronic acid hydrochloride is used as a reactant for the preparation of small molecules with a trihydroxybenzene motif. These molecules serve as pan-selectin antagonists, which have potential anti-inflammatory properties. This makes them valuable in the development of new drugs to treat various inflammatory conditions.
Used in Analytical Chemistry:
In the field of analytical chemistry, (2-Aminophenyl)boronic acid hydrochloride is used as a reactant for the preparation of designed boronate ligands. These ligands are specifically tailored for glucose-selective holographic sensors, enabling the detection and measurement of glucose levels in various samples. This application is particularly relevant in the development of diagnostic tools for monitoring blood sugar levels in patients with diabetes.
Check Digit Verification of cas no
The CAS Registry Mumber 863753-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,7,5 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 863753-30:
(8*8)+(7*6)+(6*3)+(5*7)+(4*5)+(3*3)+(2*3)+(1*0)=194
194 % 10 = 4
So 863753-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H8BNO2.ClH/c8-6-4-2-1-3-5(6)7(9)10;/h1-4,9-10H,8H2;1H
