1029716-94-6 Usage
General Description
3,5-Difluoro-4-carboxyphenylboronic acid is an organic compound and a derivative of boronic acid. The presence of the boronic acid group enables this chemical to form covalent bonds with other compounds, often used for specialized synthesis in organic chemistry. It is commonly used in the synthesis of various chemical and pharmaceutical products. The fluorine substitutions on the phenyl ring enhance its electron-withdrawing properties, increasing the chemical's overall reactivity. Additionally, the carboxy functional group allows this compound to participate in carboxylation reactions. Overall, this compound plays a crucial part in organic synthesis due to its unique physical and chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1029716-94-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,9,7,1 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1029716-94:
(9*1)+(8*0)+(7*2)+(6*9)+(5*7)+(4*1)+(3*6)+(2*9)+(1*4)=156
156 % 10 = 6
So 1029716-94-6 is a valid CAS Registry Number.
1029716-94-6Relevant articles and documents
Ortho-substituted aryl monoboronic acids have improved selectivity for d-glucose relative to d-fructose and l-lactate
Hansen,Christensen,Solling,Jakobsen,Hoeg-Jensen
, p. 1334 - 1340 (2011)
Ortho-substituted aryl monoboronic acids have been found to have improved selectivity for d-glucose compared to d-fructose and l-lactate. These findings are supported by computational studies on the B3LYP/6-31G(d) level using Gaussian. This finding is of
