220151-21-3 Usage
Uses
Used in Organic Synthesis:
Ethyl 1-bromo-4-(2-bromoethyl)-4a,5,6,7,8,8a-hexahydronaphthalene-2-carboxylate is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure, which includes bromine atoms and an ethyl group, allows it to participate in a range of chemical reactions, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, ethyl 1-bromo-4-(2-bromoethyl)-4a,5,6,7,8,8a-hexahydronaphthalene-2-carboxylate is used as a research compound to explore its potential applications in drug development. Its structural features may contribute to the discovery of new pharmaceutical agents, particularly those targeting specific biological pathways or mechanisms.
Used in Chemical Processes:
Ethyl 1-bromo-4-(2-bromoethyl)-4a,5,6,7,8,8a-hexahydronaphthalene-2-carboxylate may also be employed in other chemical processes where its reactivity and structural attributes are advantageous. This can include applications in material science, where it could be used to develop new types of polymers or other materials with unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 220151-21-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,5 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 220151-21:
(8*2)+(7*2)+(6*0)+(5*1)+(4*5)+(3*1)+(2*2)+(1*1)=63
63 % 10 = 3
So 220151-21-3 is a valid CAS Registry Number.
220151-21-3Relevant academic research and scientific papers
AMP deaminase inhibitors. 5. Design, synthesis, and SAR of a highly potent inhibitor series
Kasibhatla,Bookser,Xiao,Erion
, p. 613 - 618 (2007/10/03)
A highly potent AMP deaminase (AMPDA) inhibitor series was discovered by replacing the N3 substitutents of the two lead AMPDA inhibitor series with a conformationally restricted group. The most potent compound, 3-[2-(3-carboxy-4-bromo-5,6,7,8-tetrahydrona
Discovery of AMP mimetics that exhibit high inhibitory potency and specificity for AMP deaminase
Erion, Mark D.,Kasibhatla, Srinivas Rao,Bookser, Brett C.,Van Poelje, Paul D.,Reddy, M. Rami,Gruber, Harry E.,Appleman, James R.
, p. 308 - 319 (2007/10/03)
The first potent, specific, and cell-penetrable AMP deaminase (AMPDA) inhibitors were discovered through an investigation of 3-substituted 3,6,7,8-tetrahydroimidazo[4,5-d][1,3]diazepin-8-ol analogues. Inhibition constants for the most potent inhibitors we
