586414-93-9 Usage
Uses
Used in Pharmaceutical Industry:
rel-5-Chloro-N-[2-[4-[[[[[(1R,2R)-2-hydroxycyclohexyl]aMino]carbonyl]aMino]sulfonyl]phenyl]ethyl]-2-MethoxybenzaMide is used as a pharmaceutical compound for its potential therapeutic applications. rel-5-Chloro-N-[2-[4-[[[[[(1R,2R)-2-hydroxycyclohexyl]aMino]carbonyl]aMino]sulfonyl]phenyl]ethyl]-2-MethoxybenzaMide's diverse functional groups allow for interactions with various biological targets, making it a promising candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, rel-5-Chloro-N-[2-[4-[[[[[(1R,2R)-2-hydroxycyclohexyl]aMino]carbonyl]aMino]sulfonyl]phenyl]ethyl]-2-MethoxybenzaMide can be utilized as a starting material or intermediate for the synthesis of other complex molecules. Its unique structure and functional groups make it an interesting subject for further exploration and modification.
Used in Material Science:
rel-5-Chloro-N-[2-[4-[[[[[(1R,2R)-2-hydroxycyclohexyl]aMino]carbonyl]aMino]sulfonyl]phenyl]ethyl]-2-MethoxybenzaMide's structural features may also find applications in material science, where it could be used to develop new materials with specific properties. Its hydroxy and carbonyl groups, in particular, could be exploited to create novel polymers or other materials with tailored characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 586414-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,6,4,1 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 586414-93:
(8*5)+(7*8)+(6*6)+(5*4)+(4*1)+(3*4)+(2*9)+(1*3)=189
189 % 10 = 9
So 586414-93-9 is a valid CAS Registry Number.
586414-93-9Relevant academic research and scientific papers
Hydroxyl-Substituted sulfonylureas as potent inhibitors of specific [3H]Glyburide binding to rat brain synaptosomes
Hill, Ronald A.,Rudra, Sonali,Peng, Bo,Roane, David S.,Bounds, Jeffrey K.,Zhang, Yang,Adloo, Ahmad,Lu, Tiansheng
, p. 2099 - 2113 (2007/10/03)
We are seeking to discover potent CNS-active sulfonylureas with structural features that allow for the formation of several types of prodrugs. We report herein the syntheses of compounds comprising an initial series of hydroxyl-substituted analogues of the potent ATP-sensitive potassium channel blockers glyburide (glibenclamide) and gliquidone. Somewhat unexpectedly, several of the compounds were found to be comparably potent to glyburide as inhibitors of specific [3H]glyburide binding in rat brain preparations.
