101871-19-6 Usage
Description
(2-cyclohex-1-enyl-ethyl)-methyl-amine, with the molecular formula C11H21N, is a chemical compound that features a cyclohexene ring with an ethyl group and a methylamine group attached. (2-cyclohex-1-enyl-ethyl)-methyl-amine is recognized for its role in organic synthesis and pharmaceutical research, as well as its potential applications in the development of pharmaceutical drugs and as a precursor in the synthesis of nitrogen-containing compounds. Its biological activities and pharmacological properties have also been a subject of study, highlighting its significance in the pharmaceutical industry for further research and development.
Uses
Used in Organic Synthesis:
(2-cyclohex-1-enyl-ethyl)-methyl-amine is utilized as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows it to participate in a range of chemical reactions, facilitating the formation of new compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2-cyclohex-1-enyl-ethyl)-methyl-amine serves as a key component in research aimed at developing new drugs. Its structural properties make it a valuable candidate for the design and synthesis of pharmaceutical agents with specific therapeutic targets.
Used as a Precursor in Nitrogen-Containing Compounds Synthesis:
(2-cyclohex-1-enyl-ethyl)-methyl-amine is employed as a precursor in the synthesis of nitrogen-containing compounds. These compounds are essential in various chemical and pharmaceutical processes, and the compound's ability to contribute nitrogen to the final product makes it a useful intermediate in these syntheses.
Used in Drug Development:
(2-cyclohex-1-enyl-ethyl)-methyl-amine is used as a starting material in the development of pharmaceutical drugs. Its potential biological activities and pharmacological properties make it a promising candidate for the creation of new therapeutic agents that can address a variety of health conditions.
Used in Biological Activity and Pharmacological Property Studies:
In the realm of biological research, (2-cyclohex-1-enyl-ethyl)-methyl-amine is used to investigate its potential biological activities and pharmacological properties. This research is crucial for understanding how the compound interacts with biological systems and can lead to the discovery of new therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 101871-19-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,8,7 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101871-19:
(8*1)+(7*0)+(6*1)+(5*8)+(4*7)+(3*1)+(2*1)+(1*9)=96
96 % 10 = 6
So 101871-19-6 is a valid CAS Registry Number.
101871-19-6Relevant articles and documents
Catalytic Multisite-Selective Acetoxylation Reactions at sp2 vs sp3 C-H Bonds in Cyclic Olefins
Zang, Zhong-Lin,Zhao, Sheng,Karnakanti, Shuklachary,Liu, Cheng-Lin,Shao, Pan-Lin,He, Yun
supporting information, p. 5014 - 5017 (2016/10/14)
The first Pd-catalyzed multisite-selective acetoxylation reactions are disclosed at an unactivated alkene sp2 C-H bond versus secondary allylic sp3 C-H bond in cyclic olefins via the modulation of directing groups. The different directing groups overcome the key challenge in differentiating C-H bonds and provide a new controlling approach for site-specific C-H activation. A wide variety of substrates are readily acetoxylated under operationally simple conditions. Mechanistic studies suggest that different Pd (IV) intermediates were involved in the multisite-selective acetoxylation reactions.
