40702-53-2 Usage
Uses
Used in Pharmaceutical Industry:
1-(1-Aminocyclohexyl)ethanone is used as a building block in organic synthesis for the development of new pharmaceutical compounds. Its unique structure allows for the creation of diverse molecules with potential therapeutic applications.
Used in Research:
In the research field, 1-(1-Aminocyclohexyl)ethanone serves as a reagent in the preparation of other compounds, facilitating the advancement of scientific knowledge and the discovery of novel substances with various applications.
Used in Chemical Synthesis:
1-(1-Aminocyclohexyl)ethanone is employed as a key component in chemical synthesis, where it contributes to the production of a wide range of compounds for different industries.
Used in Medicinal Chemistry:
Due to its unique structure and properties, 1-(1-Aminocyclohexyl)ethanone may have potential applications in medicinal chemistry, where it could be used to design and synthesize new drugs with specific therapeutic targets.
It is crucial to handle 1-(1-Aminocyclohexyl)ethanone with care, as it may possess hazardous properties, and its use should adhere to proper safety precautions.
Check Digit Verification of cas no
The CAS Registry Mumber 40702-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,0 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40702-53:
(7*4)+(6*0)+(5*7)+(4*0)+(3*2)+(2*5)+(1*3)=82
82 % 10 = 2
So 40702-53-2 is a valid CAS Registry Number.
40702-53-2Relevant academic research and scientific papers
A CO2-mediated base catalysis approach for the hydration of triple bonds in ionic liquids
Han, Buxing,Ke, Zhengang,Li, Ruipeng,Liu, Zhimin,Tang, Minhao,Wang, Yuepeng,Zeng, Wei,Zhang, Fengtao,Zhao, Yanfei
supporting information, p. 9870 - 9875 (2021/12/27)
Herein, we report a CO2-mediated base catalysis approach for the activation of triple bonds in ionic liquids (ILs) with anions that can chemically capture CO2 (e.g., azolate, phenolate, and acetate), which can achieve hydration of triple bonds to carbonyl chemicals. It is discovered that the anion-complexed CO2 could abstract one proton from proton resources (e.g., IL cation) and transfer it to the CN or CC bonds via a six-membered ring transition state, thus realizing their hydration. In particular, tetrabutylphosphonium 2-hydroxypyridine shows high efficiency for hydration of nitriles and CC bond-containing compounds under a CO2 atmosphere, affording a series of carbonyl compounds in excellent yields. This catalytic protocol is simple, green, and highly efficient and opens a new way to access carbonyl compounds via triple bond hydration under mild and metal-free conditions.
