166374-43-2 Usage
Uses
Used in Pharmaceutical Industry:
exo-(+)-1R,2R,4S-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane dihydrochloride is used as a pharmaceutical agent for its potential therapeutic effects. The compound's unique structure allows it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, exo-(+)-1R,2R,4S-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane dihydrochloride serves as a valuable compound for studying the properties and reactivity of complex organic molecules. Its unique structure can provide insights into the design and synthesis of new molecules with specific functions.
Used in Drug Delivery Systems:
Similar to gallotannin, exo-(+)-1R,2R,4S-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane dihydrochloride can be employed in drug delivery systems to enhance its bioavailability and therapeutic outcomes. By incorporating exo-(+)-1R,2R,4S-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane dihydrochloride into various carriers, such as organic and metallic nanoparticles, its delivery and efficacy can be improved.
Used in Neuropharmacology:
As an α4β2 selective nicotinic agonist, exo-(+)-1R,2R,4S-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane dihydrochloride has potential applications in neuropharmacology. It can be used to study the interactions between nicotinic receptors and various neurotransmitters, as well as to develop new treatments for neurological disorders related to these receptors.
Check Digit Verification of cas no
The CAS Registry Mumber 166374-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,3,7 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 166374-43:
(8*1)+(7*6)+(6*6)+(5*3)+(4*7)+(3*4)+(2*4)+(1*3)=152
152 % 10 = 2
So 166374-43-2 is a valid CAS Registry Number.
166374-43-2Relevant academic research and scientific papers
The Synthesis of (+)- and (-)-Epibatidine
Fletcher, Stephen R.,Baker, Raymond,Chambers, Mark S.,Hobbs, Sarah C.,Mitchell, Paul J.
, p. 1216 - 1218 (2007/10/02)
The synthesis of the alkaloid epibatidine heptane> in enantiomeric form involving, as the critical step, reaction or 5-lithio-2-chloropyridine with N-tert-butoxycarbonyl-7-azabicycloheptan-2-one is des
