745836-29-7 Usage
Uses
Used in Pharmaceutical Research:
Salvinorin A is utilized as a research compound for studying the effects of kappa opioid receptors in the brain. Its unique mechanism of action provides valuable insights into the development of novel therapeutic agents targeting these receptors for various medical conditions.
Used in Drug Abuse Prevention and Education:
Due to its classification as a Schedule I controlled substance, salvinorin A is used as a reference in drug abuse prevention and education programs. It serves as a cautionary example of the potential dangers and legal consequences associated with the use of potent hallucinogenic substances.
Used in Forensic Toxicology:
Salvinorin A is employed as a target analyte in forensic toxicology for the detection and identification of its presence in biological samples. This aids in the investigation of drug-related incidents and the enforcement of drug control regulations.
Used in Ethnobotanical Studies:
As a naturally occurring psychoactive substance, salvinorin A is studied in the context of ethnobotany to understand its traditional uses, cultural significance, and potential applications in modern medicine and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 745836-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,8,3 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 745836-29:
(8*7)+(7*4)+(6*5)+(5*8)+(4*3)+(3*6)+(2*2)+(1*9)=197
197 % 10 = 7
So 745836-29-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO/c15-13-11-6-7-12(13)14(9-11)8-10-4-2-1-3-5-10/h1-5,11-13,15H,6-9H2
745836-29-7Relevant articles and documents
Approaches to syn-7-substituted 2-azanorbornanes as potential nicotinic agonists; synthesis of syn- and anti-isoepibatidine
Malpass, John R.,Handa, Sandeep,White, Richard
, p. 2759 - 2762 (2007/10/03)
(Chemical Equation Presented) Coupling of N-Boc-7-bromo-2-azabicyclo[2.2.1] heptane with aryl and pyridyl boronic acids incorporates aryl and heterocyclic substituents at the 7-position and leads to a preference for syn over anti stereoisomers. Incorporat
7-Substituted 2-Azabicyclo[2.2.1]heptanes as key intermediates for the synthesis of novel epibatidine analogues; synthesis of syn- and anti-Isoepiboxidine
Malpass, John R.,White, Richard
, p. 5328 - 5334 (2007/10/03)
Neighboring group participation by the 2-nitrogen in anti-7-bromo-2-benzyl- 2-azabicyclo[2.2.1]heptane allows ready nucleophilic substitution at the 7-position by C, N, O, and halogen nucleophiles and opens the way to a range of novel 7-substituted 2-azab
7-oxo-2-azabicyclo[2.2.1]heptanes as selective muscarinic receptor antagonist
-
, (2008/06/13)
The present invention relates to muscarinic receptor modulators, specifically, 7-oxo-2-azabicyclo[2.2.1]heptanes of formula (I) which are useful for the treatment of various diseases and conditions, for example, Alzheimer's disease, glaucoma, psychosis, particularly schizophrenia or schizophreniform conditions, mania, pain, bipolar disorder, depression, sleeping disorders, epilepsy, gastrointestinal motility disorders, urinary incontinence, and cognition enhancement.
