1234860-01-5 Usage
Uses
Used in Pharmaceutical Industry:
Trans-N1,N1-diMethylcyclohexane-1,2-diaMine-2HCl is used as a chelating agent for its ability to bind metal ions, which is crucial in the synthesis of various drugs. Its complexation capabilities contribute to enhancing the stability and efficacy of pharmaceutical formulations.
Used in Chemical Analysis and Separation Processes:
In the field of chemical analysis, Trans-N1,N1-diMethylcyclohexane-1,2-diaMine-2HCl is utilized as a reagent that aids in the separation and identification of metal ions through the formation of stable complexes, thereby facilitating more accurate analytical results.
Used in Organic Chemistry:
As a reagent in organic chemistry, Trans-N1,N1-diMethylcyclohexane-1,2-diaMine-2HCl is important for the preparation of complex organic molecules. Its structural features allow it to participate in a variety of chemical reactions, making it instrumental in the synthesis of intricate organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1234860-01-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,4,8,6 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1234860-01:
(9*1)+(8*2)+(7*3)+(6*4)+(5*8)+(4*6)+(3*0)+(2*0)+(1*1)=135
135 % 10 = 5
So 1234860-01-5 is a valid CAS Registry Number.
1234860-01-5Relevant academic research and scientific papers
3-(5-AMINO-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF
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Paragraph 1374; 1376, (2020/02/05)
The present disclosure provides a compound of Formula (I′): or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, wherein Ra, Rb, Rx, R1, R2, X2/su
Design and development of bioinspired guanine-based organic catalyst for asymmetric catalysis
Suez, Gal,Bloch, Victoria,Nisnevich, Gennady,Gandelman, Mark
supporting information; experimental part, p. 2118 - 2122 (2012/06/01)
Design, preparation, and studies of a family of new organic catalysts are presented. The design of the catalysts is inspired by the ability of DNA nucleobases to develop precise and explicit hydrogen bonds. We have shown that this phenomenon can be used to create a useful organic catalyst that demonstrates a recognition pattern similar to those of common organic substrates. A selected bifunctional catalyst based on a guanine structure has been shown to catalyze the conjugate addition of 1,3-dicarbonyl compounds to various nitroalkenes, providing the products in good yields and enantioselectivities.
