457065-49-5 Usage
Uses
Used in Pharmaceutical Applications:
3-Methoxy-5,5,8,8-tetraMethyl-5,6,7,8-tetrahydronaphthalen-2-aMine is used as an active pharmaceutical ingredient for [application reason], given its potential biological activity and interaction with biological systems. Its specific role in pharmaceuticals may be related to its chemical structure and properties, which could allow it to be used in the development of new drugs or therapeutic agents.
Used in Agricultural Applications:
In the agricultural industry, 3-Methoxy-5,5,8,8-tetraMethyl-5,6,7,8-tetrahydronaphthalen-2-aMine is used as a [application type], such as a pesticide or a growth regulator, for [application reason]. Its chemical properties may provide benefits in crop protection or enhancement of plant growth, although further research would be needed to confirm its effectiveness and safety in this context.
Used in Materials Science Applications:
3-Methoxy-5,5,8,8-tetraMethyl-5,6,7,8-tetrahydronaphthalen-2-aMine is used as a component in the development of new materials for [application reason] in materials science. Its unique chemical structure may contribute to the creation of advanced materials with specific properties, such as improved strength, flexibility, or chemical resistance. Further investigation is required to explore its full potential in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 457065-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,7,0,6 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 457065-49:
(8*4)+(7*5)+(6*7)+(5*0)+(4*6)+(3*5)+(2*4)+(1*9)=165
165 % 10 = 5
So 457065-49-5 is a valid CAS Registry Number.
457065-49-5Relevant academic research and scientific papers
Takahashi, Bitoku,Ohta, Kiminori,Kawachi, Emiko,Fukasawa, Hiroshi,Hashimoto, Yuichi,Kagechika, Hiroyuki
, p. 3327 - 3330 (2002)
Several 2-(arylamino)pyrimidine-5-carboxylic acids were designed as novel retinoid X receptor (RXR) antagonists. Compound 6a or 6b alone did not exhibit differentiation-inducing activity toward HL-60 cells and did not affect the activity of a retinoic acid receptor (RAR) agonist, Am80, but did inhibit the synergistic activity of an RXR agonist, PA024 (3), in the presence of Am80. The activity of 6 was ascribed to selective antagonism at the RXR site of RXR-RAR heterodimers.
Aza-retinoids as novel retinoid X receptor-specific agonists
Farmer, Luc J.,Marron, Kristen S.,Canan Koch, Stacie S.,Hwang,Kallel, E. Adam,Zhi, Lin,Nadzan, Alex M.,Robertson, Dave W.,Bennani, Youssef L.
, p. 2352 - 2356 (2007/10/03)
A new structurally simple series of potent lipophilic aza-retinoids RXR agonists has been developed. SAR studies for the N-alkyl-azadienoic acids described here demonstrate that the RXR activity profile is sensitive to the N-alkyl chain length. Further, we have expanded the work to include azadienoic acids, which exhibited many accessible conformations leading to a better understanding of the SAR around the series.
