1421697-46-2 Usage
Uses
Used in Organic Chemistry Research:
(2S)-2-[[[[(1S,2S)-2-amino-cyclohexyl]amino]thioxomethyl]amino]-N-(diphenylmethyl)-N,3,3-trimethyl-butanamide serves as a research chemical in organic chemistry, where it is used for studying the synthesis and reactions of complex organic molecules. Its unique structure allows for the exploration of new chemical pathways and mechanisms.
Used in Biochemistry Research:
In biochemistry, (2S)-2-[[[[(1S,2S)-2-aMinocyclohexyl]aMino]thioxoMethyl]aMino]-N-(diphenylMethyl)-N,3,3-triMethyl-ButanaMide is utilized for investigating its interactions with biological systems. It can be employed to study enzyme mechanisms, protein structures, and other biochemical processes, potentially leading to insights into new biological functions or the development of novel therapeutic agents.
Used in Pharmaceutical Development:
(2S)-2-[[[[(1S,2S)-2-amino-cyclohexyl]amino]thioxomethyl]amino]-N-(diphenylmethyl)-N,3,3-trimethyl-butanamide may also be used in pharmaceutical development. Its complex structure and chiral center could offer unique pharmacological properties, making it a candidate for the development of new drugs with specific therapeutic targets.
Used in Material Science:
In material science, (2S)-2-[[[[(1S,2S)-2-aMinocyclohexyl]aMino]thioxoMethyl]aMino]-N-(diphenylMethyl)-N,3,3-triMethyl-ButanaMide could be explored for its potential to form new materials with unique properties. Its ability to interact with other molecules and its structural characteristics might contribute to the creation of advanced materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1421697-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,6,9 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1421697-46:
(9*1)+(8*4)+(7*2)+(6*1)+(5*6)+(4*9)+(3*7)+(2*4)+(1*6)=162
162 % 10 = 2
So 1421697-46-2 is a valid CAS Registry Number.
1421697-46-2Relevant 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.
