132234-69-6 Usage
Uses
Used in Pharmaceutical Synthesis:
Endo-3-Boc-aminotropane is used as a precursor in the synthesis of various pharmaceuticals and psychoactive substances. Its structural similarity to cocaine allows for the development of compounds with modified properties, potentially leading to new therapeutic agents.
Used in Neurological Disorder Treatment:
Endo-3-Boc-aminotropane is used as a research compound for its potential therapeutic effects in treating neurological disorders. Its stimulant and hallucinogenic properties may offer insights into the development of new treatments for conditions such as Parkinson's disease and Alzheimer's disease.
Used in Substance Abuse Treatment:
Endo-3-Boc-aminotropane is used as a research compound in the development of treatments for substance abuse. Its potential to modulate the effects of addictive substances may contribute to the creation of new therapies for addiction recovery and relapse prevention.
Used in Psychoactive Substance Development:
Endo-3-Boc-aminotropane is used as a research compound in the development of new psychoactive substances. Its unique properties and structural characteristics may lead to the discovery of novel compounds with distinct effects on the central nervous system.
Used in Organic Synthesis:
Endo-3-Boc-aminotropane is used as a protective group in organic synthesis. The tert-butoxycarbonyl (Boc) group on the nitrogen atom can be selectively removed under mild conditions, allowing for the synthesis of various tropane alkaloid derivatives with specific functional groups and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 132234-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,3 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132234-69:
(8*1)+(7*3)+(6*2)+(5*2)+(4*3)+(3*4)+(2*6)+(1*9)=96
96 % 10 = 6
So 132234-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H24N2O2/c1-13(2,3)17-12(16)14-9-7-10-5-6-11(8-9)15(10)4/h9-11H,5-8H2,1-4H3,(H,14,16)/t9-,10+,11-
132234-69-6Relevant academic research and scientific papers
Quinolone Antibacterials: Preparation and Activity of Bridged Bicyclic Analogues of the C7-Piperazine
Kiely, John S.,Hutt, Marland P.,Culbertson, Townley P.,Bucsh, Ruth A.,Worth, Donald F.,et al.
, p. 656 - 663 (2007/10/02)
A series of quinolone and naphthyridine antibacterial agents possessing as the C7-heterocycle bicyclic 2,5-diazabicycloalkanes, where n = 2, 3 and m = 1, 2, and a series including 4-aminopiperidine and 3-amino-8-azabicyclooctanes have been prepared and evaluated in vitro and in vivo for antibacterial activity against a variety of Gramm-negative and Gramm-positive organisms.These compounds were also tested against the target enzyme bacterial DNA gyrase.All the examples investigated are nearly equipotent with the parent 7-piperazinyl analogues.Only endo-7-(3-amino-8-azabicyclooct-8-yl) -1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid displays activity that surpasses that of the piperazine parent.
