145041-54-9 Usage
Uses
Used in Pharmaceutical Research:
5,6,7,8-tetrahydro-1-(Methylthio)-5,8-Methanoisoquinoline is used as a research compound for exploring its potential biological activities. The unique structure of this heterocyclic compound suggests it may possess properties that are beneficial in the development of new pharmaceutical agents.
Used in Drug Development:
In the field of drug development, 5,6,7,8-tetrahydro-1-(Methylthio)-5,8-Methanoisoquinoline is utilized as a lead compound. Its specific chemical features, including the sulfur-containing functional group, could be instrumental in the creation of novel therapeutics, particularly if they exhibit desired pharmacological effects.
Further research is essential to determine the specific applications of 5,6,7,8-tetrahydro-1-(Methylthio)-5,8-Methanoisoquinoline in various industries, as its uses are currently under investigation due to its novel structure and potential biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 145041-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 145041-54:
(8*1)+(7*4)+(6*5)+(5*0)+(4*4)+(3*1)+(2*5)+(1*4)=99
99 % 10 = 9
So 145041-54-9 is a valid CAS Registry Number.
145041-54-9Relevant academic research and scientific papers
Synthesis of novel rigid norbornylogous spacers bearing heterocyclic ligands for the investigation of long-range intramolecular electron transfer involving metal centres
Golka,Keyte,Paddon-Row
, p. 7663 - 7678 (2007/10/02)
The synthesis of some novel 1,4-dimethoxynaphthalene-bridge-heterocycle systems is described. In these systems, the naphthalene and heterocyclic groups are fused to a rigid bridge consisting of linearly fused norbornyl and bicyclo[2.2.0]hexyl groups. Bridges used herein have relays of 2-, 4-, and 6-bonds long. The heterocycle is either 3,6-di(2'-pyridyl)-pyridazino, or pyrido and was attached to the bridge by annulation methods. The pyridazine systems, 2(m,n), were synthesized via Diels-Alder reaction of 3,6-di(2'-pyridyl)-1,2,4,5-tetrazine with the alkenes, 13 and 6(m,n), and subsequent aromatization of the adducts with DDQ. Pyridine annulation was successfully carried out using two different methods: (i) Boger pyridine annulation of ketones, 11, 20b, and 21b, (with 1,2,4-triazine and pyrrolidine): (ii) Diels-Alder reaction of alkenes 13 and 6(m,n) with 3-thiomethyl-1,2,4-triazine, followed by Raney nickel reductive desulfurization of the aromatized adducts. The synthesis of Ru(II)(2,2'-bipyridyl)2 complexes of the pyridazino systems 9(m,n) and 10, is also described.
