85613-27-0 Usage
Imidazole ring
A five-membered ring structure consisting of five carbon atoms and two nitrogen atoms.
2-[4-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]phenyl] group
A phenyl ring attached to a dioxolane ring through a methoxy group.
Potential applications
Organic synthesis, pharmaceuticals, and material science.
Versatile biological activities
The imidazole ring is known for its ability to interact with various biological systems.
Coordination chemistry capabilities
The imidazole ring can form coordination complexes with metal ions, enhancing its utility in various applications.
Building block for complex organic molecules
The compound can be used as a starting material for the synthesis of a wide range of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 85613-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,1 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85613-27:
(7*8)+(6*5)+(5*6)+(4*1)+(3*3)+(2*2)+(1*7)=140
140 % 10 = 0
So 85613-27-0 is a valid CAS Registry Number.
85613-27-0Relevant academic research and scientific papers
β1-Selective adrenoceptor antagonists: Examples of the 2-[4-[3-(substituted-amino)-2-hydroxypropoxy]phenyl]imidazole class
Baldwin,Denny,Hirschmann,Freedman,Ponticello,Gross,Sweet
, p. 950 - 957 (2007/10/02)
A series of 2-[4-[3-(substituted-amino)-2-hydroxypropoxy]phenyl]imidazoles is described. The compounds were investigated in vitro for β-adrenoceptor antagonism, and several examples were found to be selective for the β1-adrenoceptor. The structure-activity relationship exhibited by this series of compounds is discussed. (S)-2-[p-[3-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-2-hydroxypropoxy]phenyl] -4-(2-thienyl)imidazole [(S)-13] was over 100 times more selective than atenolol for the β1-adrenergic receptor and has been selected for in-depth studies.
