1421052-39-2 Usage
Uses
Used in Pharmaceutical Industry:
(2S)-2-[[[[(1R,2R)-2-aMinocyclohexyl]aMino]thioxoMethyl]aMino]-N-(diphenylMethyl)-N,3,3-triMethyl-ButanaMide is used as a potential pharmaceutical compound for its unique structure and functional groups, which may offer novel therapeutic properties and applications.
Used in Biotechnology Industry:
(2S)-2-[[[[(1R,2R)-2-aMinocyclohexyl]aMino]thioxoMethyl]aMino]-N-(diphenylMethyl)-N,3,3-triMethyl-ButanaMide is used as a component in biotechnological processes, where its chiral nature and functional groups can be utilized for the development of new bioactive molecules or as a building block for more complex structures.
Used in Materials Science:
(2S)-2-[[[[(1R,2R)-2-aMinocyclohexyl]aMino]thioxoMethyl]aMino]-N-(diphenylMethyl)-N,3,3-triMethyl-ButanaMide is used in materials science for the development of new materials with unique properties, such as chiral polymers or self-assembling systems, due to its complex structure and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 1421052-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,0,5 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1421052-39:
(9*1)+(8*4)+(7*2)+(6*1)+(5*0)+(4*5)+(3*2)+(2*3)+(1*9)=102
102 % 10 = 2
So 1421052-39-2 is a valid CAS Registry Number.
1421052-39-2Relevant academic research and scientific papers
Enantioselective formal aza-Diels-Alder reactions of enones with cyclic imines catalyzed by primary aminothioureas
Lalonde, Mathieu P.,McGowan, Meredeth A.,Rajapaksa, Naomi S.,Jacobsen, Eric N.
, p. 1891 - 1894 (2013/04/10)
A highly enantio- and diastereoselective synthesis of indolo- and benzoquinolizidine compounds has been developed through the formal aza-Diels-Alder reaction of enones with cyclic imines. This transformation is catalyzed by a new bifunctional primary aminothiourea that achieves simultaneous activation of both the enone and imine reaction components.
