79150-46-2 Usage
Uses
Used in Asymmetric Synthesis:
(1R,2R)-N,N,N'-triMethyl-1,2-diaMinocyclohexane is used as a chiral ligand in asymmetric synthesis for its ability to induce selectivity in chemical reactions, leading to the preferential formation of one enantiomer over another. This is crucial in the production of enantiomerically pure compounds, which is essential in pharmaceuticals where different enantiomers can have different biological activities.
Used in Catalysts for Organic Reactions:
In the field of catalysis, (1R,2R)-N,N,N'-triMethyl-1,2-diaMinocyclohexane serves as a catalyst to accelerate various organic reactions. Its chiral nature allows it to selectively influence the course of reactions, enhancing the yield and selectivity of desired products, which is particularly important in the synthesis of complex organic molecules.
Used in Pharmaceutical Synthesis:
(1R,2R)-N,N,N'-triMethyl-1,2-diaMinocyclohexane is utilized in the synthesis of pharmaceuticals as a key intermediate or building block. Its ability to form complex molecules with high selectivity makes it a valuable component in the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, (1R,2R)-N,N,N'-triMethyl-1,2-diaMinocyclohexane is employed in the synthesis of agrochemicals, such as pesticides and herbicides. Its chiral properties enable the creation of highly selective agents that can target specific pests or weeds without harming beneficial organisms or the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 79150-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79150-46:
(7*7)+(6*9)+(5*1)+(4*5)+(3*0)+(2*4)+(1*6)=142
142 % 10 = 2
So 79150-46-2 is a valid CAS Registry Number.
79150-46-2Relevant academic research and scientific papers
Design, synthesis, and biological evaluation of pirenzepine analogs bearing a 1,2-cyclohexanediamine and perhydroquinoxaline units in exchange for the piperazine ring as antimuscarinics
Minarini, Anna,Marucci, Gabriella,Bellucci, Cristina,Giorgi, Gianluca,Tumiatti, Vincenzo,Bolognesi, Maria Laura,Matera, Riccardo,Rosini, Michela,Melchiorre, Carlo
, p. 7311 - 7320 (2008/12/22)
Pirenzepine (2) is one of the most selective muscarinic M1 versus M2 receptor antagonists known. A series of 2 analogs, in which the piperazyl moiety was replaced by a cis- and trans-cyclohexane-1,2-diamine (3-6) or a trans- and cis-
