81094-63-5 Usage
Chemical structure
A complex molecular structure belonging to the family of benzoxazocin-3-one derivatives.
Application
Primarily used in medicinal chemistry for research purposes.
Potential use
Shown potential in the development of new pharmaceutical drugs.
Fields of interest
Particularly in the fields of neuroscience and psychiatry.
Unique features
Its unique structure and pharmacological properties make it an interesting target for further investigation and potential drug development.
Research status
Due to its complex nature, further research is needed to fully understand its potential applications and therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 81094-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,9 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81094-63:
(7*8)+(6*1)+(5*0)+(4*9)+(3*4)+(2*6)+(1*3)=125
125 % 10 = 5
So 81094-63-5 is a valid CAS Registry Number.
81094-63-5Relevant academic research and scientific papers
Hathaway,Nichols,Nichols,Yim
, p. 535 - 538 (1982)
A new stimulant compound, 1,2-dihydro-2-naphthalenamine (2-amino-1,2-dihydronaphthalene, 2-ADN), was prepared as an analogue of amphetamine and of 2-aminotetralin. The optical isomers of 2-ADN were obtained by chemical resolution, and the absolute configuration was determined to be R-(+) and S-(-). Preliminary pharmacological evaluation revealed that racemic 2-ADN is approximately one-fourth as potent as (+)-amphetamine as a stimulant in mice. The S-(-) isomer of 2-ADN was found to be solely responsible for the stimulant effects of the racemate. Both reserpine and α-methyl-p-tyrosine antagonized the stimulation produced by 2-ADN.
