1161012-23-2 Usage
General Description
2-amino-N,N-dimethyl-2-phenylacetamide, also known as dimethylamphetamine, is a chemical compound with the molecular formula C11H16N2O. It is a derivative of amphetamine and has been used in the field of medicinal chemistry as a potential central nervous system stimulant and anorectic agent. The compound is a white crystalline powder that is slightly soluble in water and has a melting point of around 123-126°C. Its structural similarity to amphetamines suggests that it may have similar biological effects, but its specific pharmacological properties and potential uses are still under investigation. Due to its potential stimulant effects, it may have the ability to increase the levels of certain neurotransmitters in the brain, leading to increased energy and alertness. However, further research is needed to fully understand its pharmacological potential and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 1161012-23-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,1,0,1 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1161012-23:
(9*1)+(8*1)+(7*6)+(6*1)+(5*0)+(4*1)+(3*2)+(2*2)+(1*3)=82
82 % 10 = 2
So 1161012-23-2 is a valid CAS Registry Number.
1161012-23-2Relevant articles and documents
A class of α-amino acids-derived multifunctional amidophosphane precatalysts: application to the highly enantio- and diastereoselective silver(I)-catalyzed 1,3-dipolar cycloaddition reaction
Hou, Yihui,Zhou, Zhipeng,Liu, Pingle,Wang, Jiankang,Hou, Qinglin,Wen, Pushan,Wang, Haifei
, p. 930 - 938 (2017/07/11)
A class of multifunctional amidophosphanes derived from chiral α-amino acids have been developed with two amide bonds, a tertiary amine and a phosphine. In combination with Ag(I) salts, these amidophosphanes have been demonstrated as highly efficient multifunctional catalysts in the asymmetric 1,3-dipolar cycloaddition of azomethine ylides as well as the three-component reaction of the α-iminoesters in situ generated. Under optimal conditions, highly functionalized endo-8 pyrrolidines were obtained with good to excellent yields (up to 99% yield) and enantioselectivities (up to 98% ee).
CARBONYLAMINO PYRROLOPYRAZOLES, POTENT KINASE INHIBITORS
-
Page/Page column 63-64, (2009/12/28)
Carbonylamino Pyrrolopyrazole compounds of formula I, compositions including these compounds and methods of their use are provided. Preferred compounds of formula I have activity as protein kinase inhibitors, including as inhibitors of PAK4.
PYRROLOPYRAZOLES, POTENT KINASE INHIBITORS
-
Page/Page column 68-71, (2008/06/13)
-
