47216-53-5 Usage
Molecular structure
A complex structure that includes a 1,2,3,4-tetrahydroisoquinoline backbone, a 4-chlorobenzyl group, and two methoxy groups.
Medicinal chemistry
The compound may be utilized in the development of pharmaceuticals due to its potentially unique biological activities.
Organic synthesis
It may have applications in organic synthesis due to its specific structure and reactivity.
Chemical research
The compound may be used for further research into its potential uses and interactions with biological systems.
Biological activities
The compound's structure suggests that it may have interactions with biological systems, making it a candidate for drug development or further research.
Chemical reactivity
The presence of the 4-chlorobenzyl group and methoxy groups may contribute to the compound's reactivity in chemical reactions.
1,2,3,4-Tetrahydroisoquinoline backbone
The central core of the molecule, providing a foundation for the attachment of other functional groups.
4-chlorobenzyl group
A chlorine atom attached to a benzyl group, which may influence the compound's reactivity and interactions with biological systems.
Potential drug development
The compound's unique structure and potential biological activities make it a candidate for further research and development in the pharmaceutical industry.
Research focus
Further investigation into the compound's interactions with biological systems, its reactivity in chemical reactions, and its potential applications in medicinal chemistry and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 47216-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,2,1 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 47216-53:
(7*4)+(6*7)+(5*2)+(4*1)+(3*6)+(2*5)+(1*3)=115
115 % 10 = 5
So 47216-53-5 is a valid CAS Registry Number.
47216-53-5Relevant academic research and scientific papers
Enantioselective Oxidative Aerobic Dealkylation of N-Ethyl Benzylisoquinolines by Employing the Berberine Bridge Enzyme
Gandomkar, Somayyeh,Fischereder, Eva-Maria,Schrittwieser, Joerg H.,Wallner, Silvia,Habibi, Zohreh,Macheroux, Peter,Kroutil, Wolfgang
, p. 15051 - 15054 (2016/01/25)
N-Dealkylation methods are well described for organic chemistry and the reaction is known in nature and drug metabolism; however, to our knowledge, enantioselective N-dealkylation has not been yet reported. In this study, exclusively the (S)-enantiomers o
Oxidation of 1-benzyldihydroisoquinolines or 1- benzyltetrahydroisoquinolines with dioxygen to 1-benzoylisoquinolines
Gan, Haifeng,Lu, Yunyu,Huang, Yue,Ni, Lijun,Xu, Jinyi,Yao, Hequan,Wu, Xiaoming
body text, p. 1320 - 1324 (2011/04/15)
An environmental-benign methodology to synthesize 1-benzoylisoquinolines from 1-benzyl-3, 4-dihydroisoquinolines or 1-benzyl-1,2,3,4- tetrahydroisoquinolines using dioxygen as an oxidant was developed. This methodology in combination with Bischler-Napieralski reaction leads to a facile synthesis of 1-benzoylisoquinolines from phenylacetic acids and phenylethanamines.
Synthesis of 6,7-dimethoxy-1-halobenzyl-1,2,3,4-tetrahydroisoquinolines
Cho, Su-Dong,Kweon, Deok-Heon,Kang, Young-Jin,Lee, Sang-Gyeong,Lee, Woo Song,Yoon, Yong-Jin
, p. 1151 - 1156 (2007/10/03)
Some 6,7-dimethoxy-1-halobenzyl-1,2,3,4-tetrahydroisoquinolines were synthesized from 2-(3,4-dimethoxyphenyl)ethylamine and halophenylacetic acids in three steps in good yield.
