168902-82-7 Usage
Uses
Used in Pharmaceutical Research:
(S)-4,5-DIMETHOXY-INDAN-1-YLAMINE is used as a research compound for its potential role in the development of new psychoactive substances. Its unique chemical structure and properties make it a valuable tool for scientists and researchers working in drug discovery and development.
Used in Drug Discovery and Development:
(S)-4,5-DIMETHOXY-INDAN-1-YLAMINE is used as a chemical compound in the field of drug discovery and development, where its interactions with receptors in the central nervous system are of particular interest. (S)-4,5-DIMETHOXY-INDAN-1-YLAMINE's potential pharmacological activity could lead to the creation of novel treatments for various conditions.
Used in Central Nervous System Research:
In the field of neuroscience, (S)-4,5-DIMETHOXY-INDAN-1-YLAMINE is used as a research compound to study its interactions with receptors in the central nervous system. This research could potentially contribute to a better understanding of the compound's pharmacological activity and its potential applications in the treatment of neurological disorders.
Used in Organic Chemistry:
(S)-4,5-DIMETHOXY-INDAN-1-YLAMINE is also used as a chemical compound in the field of organic chemistry, where its indane ring structure and methoxy functional groups can be further explored for the synthesis of new molecules and the development of innovative chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 168902-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,9,0 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 168902-82:
(8*1)+(7*6)+(6*8)+(5*9)+(4*0)+(3*2)+(2*8)+(1*2)=167
167 % 10 = 7
So 168902-82-7 is a valid CAS Registry Number.
168902-82-7Relevant academic research and scientific papers
Method for preparing optically active 1-aminoindan derivatives
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, (2008/06/13)
Novel derivatives of 1-aminoindan and their salts are described. Optically active 1-aminoindan derivatives are prepared by reacting a N-benzyl analog of the desired compound with an enantiomer of mandelic acid. Parkinson's disease, dementia, epilepsy, con
