721395-52-4 Usage
Structure
Contains a phenylboronic acid group linked to a diphenylprop-2-enyloxyphenyl group
Type of compound
Boronic acid derivative
Bonding ability
Can form reversible covalent bonds with diols
Usage
As a building block in the synthesis of more complex organic molecules
Boronic acid functionality
Participates in Suzuki coupling reactions and other transformations in organic chemistry
Pharmaceutical potential
Studied for the treatment of diabetes and cancer
Check Digit Verification of cas no
The CAS Registry Mumber 721395-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,1,3,9 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 721395-52:
(8*7)+(7*2)+(6*1)+(5*3)+(4*9)+(3*5)+(2*5)+(1*2)=154
154 % 10 = 4
So 721395-52-4 is a valid CAS Registry Number.
721395-52-4Relevant academic research and scientific papers
Organolead-mediated arylations: 2-(3,3-diphenylallyloxy)phenyllead triacetate as an internal free-radical-trap-containing reagent
Fedorov, Alexey Yu.,Finet, Jean-Pierre
, p. 2040 - 2045 (2007/10/03)
2-(3,3-Diphenylprop-2-enyloxy)phenyllead triacetate, an arylating reagent containing an internal free radical trap, was synthesised and its behaviour studied in base-catalysed C-arylation reactions and in copper-catalysed N-arylation reactions. The absence of benzofuran derivatives among the products of C- and N-arylation reactions excludes the involvement of radical species in these two processes. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
