1148044-35-2 Usage
Uses
Due to the limited information available on the uses of 2,7-Diazaspiro[4.4]nonane-1,3-dione, 2-(phenylMethyl)-, it is not possible to provide a comprehensive list of its applications. However, based on its classification as an organonitrogen compound and its potential properties, it can be inferred that it may have applications in the following areas:
Used in Pharmaceutical Industry:
2,7-Diazaspiro[4.4]nonane-1,3-dione, 2-(phenylMethyl)may be used as a chemical intermediate or a building block in the synthesis of pharmaceutical compounds. Its organonitrogen nature could contribute to the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
2,7-Diazaspiro[4.4]nonane-1,3-dione, 2-(phenylMethyl)could be utilized in academic or industrial research settings to study its chemical properties, reactivity, and potential interactions with other molecules. Understanding its behavior could lead to the discovery of new chemical reactions or the development of novel materials.
Used in Material Science:
2,7-Diazaspiro[4.4]nonane-1,3-dione, 2-(phenylMethyl)may have potential applications in the development of new materials, such as polymers or composites, due to its unique structure and properties. Its incorporation into these materials could lead to improved performance or new functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 1148044-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,8,0,4 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1148044-35:
(9*1)+(8*1)+(7*4)+(6*8)+(5*0)+(4*4)+(3*4)+(2*3)+(1*5)=132
132 % 10 = 2
So 1148044-35-2 is a valid CAS Registry Number.
1148044-35-2Relevant academic research and scientific papers
Preparation and characterization of N-(3-pyridinyl) spirocyclic diamines as ligands for nicotinic acetylcholine receptors
Sippy, Kevin B.,Anderson, David J.,Bunnelle, William H.,Hutchins, Charles W.,Schrimpf, Michael R.
scheme or table, p. 1682 - 1685 (2009/11/30)
Several N-pyridin-3-yl spirobicyclic diamines, designed as conformationally restricted analogs of tebanicline (ABT-594), were synthesized as novel ligands for nicotinic acetylcholine receptors (nAChR). The spirocyclic compounds exhibited weaker binding affinity, than other constrained analogs in accord with a pharmacophore model. Nevertheless, some (1a, 1b) possessed (partial) agonist potencies comparable to nicotine at the α4β2 subtype, but with greatly improved selectivity relative to the α3β4* nAChR.
