103698-26-6 Usage
Class
boronic acids
Molecular weight
271.143 g/mol
Common use
as a reagent in the Suzuki-Miyaura coupling reaction
Property
ability to form stable complexes with diols and other Lewis bases
Analytical applications
valuable tools in the development of sensors
Therapeutic potential
investigated for its potential as a treatment for diabetes due to insulin-mimetic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 103698-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,9 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103698-26:
(8*1)+(7*0)+(6*3)+(5*6)+(4*9)+(3*8)+(2*2)+(1*6)=126
126 % 10 = 6
So 103698-26-6 is a valid CAS Registry Number.
103698-26-6Relevant articles and documents
Strategies towards the synthesis of 6-N,N-diethylcarbamyloxy-1,4-dimethoxy- 7-naphthylboronic acid
Ameer,Green, Ivan R.,Krohn,Sitoza
, p. 3041 - 3057 (2008/02/12)
After acetylation, condensation between Danishefsky's diene and benzoquinone afforded a stable methoxytriacetoxydihydronaphthalene intermediate, which was subsequently transformed by the Snieckus DOM protocol into the regiospecific 7-naphthylboronic acid.
