80460-73-7 Usage
Uses
Different sources of media describe the Uses of 80460-73-7 differently. You can refer to the following data:
1. suzuki reaction
2. 4-Aminophenylboronic acid hydrochloride can be used to prepare:The modified reduced graphene composite material used as a sugar sensor to detect the analyte in fruit juice.The modified carbon electrode adsorbed with aminophenol, used for the detection of NADH and H2O2.The boron, nitrogen, and sulfur-doped carbon dot sensor, which in turn can be used for the detection of ascorbic acid.
General Description
May contain varying amounts of anhydride
Check Digit Verification of cas no
The CAS Registry Mumber 80460-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,6 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80460-73:
(7*8)+(6*0)+(5*4)+(4*6)+(3*0)+(2*7)+(1*3)=117
117 % 10 = 7
So 80460-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H8BNO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H,8H2
80460-73-7Relevant articles and documents
Virtues of Volatility: A Facile Transesterification Approach to Boronic Acids
Hinkes, Stefan P.A.,Klein, Christian D.P.
supporting information, p. 3048 - 3052 (2019/05/10)
Boronic acids are an increasingly important compound class for many applications, including C-C bond formation reactions, medicinal chemistry, and diagnostics. The deprotection of boronic ester intermediates is frequently a problematic and inefficient step in boronic acid syntheses. We describe an approach that highly facilitates this transformation by leveraging the volatility of methylboronic acid and its diol esters. The method is performed under mild conditions, provides high yields, and eliminates cumbersome and problematic purification steps.
